NDC Product
Human Prescription DrugCreon NDC 0032-1203
- Generic Name
- Pancrelipase
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- BLA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Cetyl Alcohol, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 936JST6JCN.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 36653-82-4 and the RxNorm Concept ID (RxCUI) 20615. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
CETYL ALCOHOL
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
936JST6JCN
The specific atomic composition represented as a molecular structure string.
InChIKey
C16H34O International Chemical Identifier digital signature for unique molecular identification.
SMILES String
BXWNKGSJHAJOGX-UHFFFAOYSA-N Line notation for describing the chemical structure and connectivity of atoms.
NCI Thesaurus
National Cancer Institute reference terminology for clinical and research data.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
OCCCCCCCCCCCCCCCC
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Cetyl Alcohol. Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.
FDA Official Name
CETYL ALCOHOL
OF
Common Names & Synonyms
1-HEXADECANOL [FHFI]
CN
ALCOHOL CETYLICUS [WHO-IP LATIN]
CN
CETANOL [JAN]
CN
CETYL ALCHOL
CN
CETYL ALCOHOL [EP MONOGRAPH]
CN
CETYL ALCOHOL [HSDB]
CN
CETYL ALCOHOL [II]
CN
CETYL ALCOHOL [MART.]
CN
CETYL ALCOHOL [MI]
CN
CETYL ALCOHOL [USP-RS]
CN
CETYL ALCOHOL [VANDF]
CN
CETYL ALCOHOL [WHO-DD]
CN
CETYL ALCOHOL [WHO-IP]
CN
N-1-HEXADECANOL
CN
N-HEXADECANOL
CN
PALMITIC ALCOHOL
CN
Systematic Nomenclature
1-HEXADECANOL
SYS
CETANOL
SYS
HEXADECANOL
SYS
HEXADECYL ALCOHOL
SYS
PALMITYL ALCOHOL
SYS
Technical Codes
FEMA NO. 2554
CD
NSC-4194
CD
NDC Products Containing CETYL ALCOHOL
This unique ingredient identifier is listed as an ingredient or substance in the following products in the NDC directory:
Manufacturer Quick Index
Note: Due to the high number of listings (500), only Active Listings are currently displayed. Display is limited to the first 200 products.
Showing 200 active products
AbbVie Inc.
Active Listing
NDC Product
Human Prescription DrugCreon NDC 0032-1206
- Generic Name
- Pancrelipase
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugCreon NDC 0032-1212
- Generic Name
- Pancrelipase
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugCreon NDC 0032-1224
- Generic Name
- Pancrelipase
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugCreon NDC 0032-3016
- Generic Name
- Pancrelipase
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- BLA
Active Listing
Access Business Group LLC
NDC Product
Human Otc DrugSatinique Anti Dandruff Scalp And Hair NDC 10056-536
- Generic Name
- Salicylic Acid
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Actavis Pharma, Inc.
NDC Product
Human Prescription DrugClotrimazole And Betamethasone Dipropionate NDC 0472-0379
- Generic Name
- Clotrimazole And Betamethasone Dipropionate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPimecrolimus NDC 0591-2944
- Generic Name
- Pimecrolimus
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
Amneal Pharmaceuticals of New York LLC
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0115-1736
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0115-1737
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0115-1738
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0115-1739
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0115-1740
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0115-1741
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Sulfate Extended-release NDC 0115-9927
- Generic Name
- Dextroamphetamine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Sulfate Extended-release NDC 0115-9928
- Generic Name
- Dextroamphetamine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Sulfate Extended-release NDC 0115-9929
- Generic Name
- Dextroamphetamine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Bausch Health US LLC
NDC Product
Human Prescription DrugRenova NDC 0187-5150
- Generic Name
- Tretinoin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA
Active Listing
Beiersdorf Inc
NDC Product
Human Otc DrugEucerin Daily Protection Face NDC 10356-323
- Generic Name
- Ensulizole, Octinoxate, Octisalate, Titanium Dioxide, Zinc O...
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEucerin Daily Hydration NDC 10356-335
- Generic Name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEucerin Skin Calming Itch Relief Treatment NDC 10356-357
- Generic Name
- Menthol
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEucerin Eczema Relief Body NDC 10356-365
- Generic Name
- Oatmeal
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEucerin Eczema Relief Flare Up Treatment NDC 10356-371
- Generic Name
- Oatmeal
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEucerin Eczema Relief Hydrogel NDC 10356-390
- Generic Name
- Oatmeal
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Blistex Inc
NDC Product
Human Otc DrugBlistex Medicated Lip Balm NDC 10157-1119
- Generic Name
- Dimethicone, Octinoxate, And Octisalate
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBlistex Medicated Mint Balm NDC 10157-1120
- Generic Name
- Dimethicone, Octinoxate, And Octisalate
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBlistex Medicated Berry Balm NDC 10157-1121
- Generic Name
- Dimethicone, Octinoxate, And Octisalate
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMedicated Peppermint Lip Balm NDC 10157-4104
- Generic Name
- Dimethicone, Unspecified, Octinoxate, And Octisalate
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBlistex Medicated Lip Balm Variety Pack (blistex Medicated Berry Lip Balm, Blistex Medicated Lip Balm, Blistex Medicated Mint Lip Balm) NDC 10157-9908
- Generic Name
- Dimethicone, Octinoxate, And Octisalate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBlistex Medicated Lip Balm Variety Pack (blistex Medicated Berry Lip Balm, Blistex Medicated Lip Balm, Blistex Medicated Lip) NDC 10157-9910
- Generic Name
- Dimethicone, Octinoxate, Octisalate, Camphor (synthetic), Me...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Blistex Inc.
NDC Product
Human Otc DrugLip Medex Lip Balm NDC 10157-1194
- Generic Name
- Petrolatum, Camphor (synthetic), Menthol, Unspecified Form, ...
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugOdor-eaters Athletes Foot NDC 10157-3100
- Generic Name
- Tolnaftate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBlistex Medicated NDC 10157-9951
- Generic Name
- Dimethicone, Camphor (synthetic), Menthol, And Phenol
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Cosette Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugFluocinolone Acetonide NDC 0713-0223
- Generic Name
- Fluocinolone Acetonide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluocinolone Acetonide NDC 0713-0224
- Generic Name
- Fluocinolone Acetonide
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTriamcinolone Acetonide NDC 0713-0225
- Generic Name
- Triamcinolone Acetonide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTriamcinolone Acetonide NDC 0713-0226
- Generic Name
- Triamcinolone Acetonide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBetamethasone Valerate NDC 0713-0326
- Generic Name
- Betamethasone Valerate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBetamethasone Valerate NDC 0713-0327
- Generic Name
- Betamethasone Valerate
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCiclopirox Olamine NDC 0713-0638
- Generic Name
- Ciclopirox Olamine
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHalobetasol Propionate NDC 0713-0640
- Generic Name
- Halobetasol Propionate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBetamethasone Dipropionate NDC 0713-0659
- Generic Name
- Betamethasone Dipropionate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluocinonide NDC 0713-0664
- Generic Name
- Fluocinonide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTriamcinolone Acetonide NDC 0713-0676
- Generic Name
- Triamcinolone Acetonide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluocinolone Acetonide NDC 0713-0709
- Generic Name
- Fluocinolone Acetonide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
Crown Laboratories
NDC Product
Human Prescription DrugAlacort NDC 0316-0126
- Generic Name
- Hydrocortisone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAlacort NDC 0316-0128
- Generic Name
- Hydrocortisone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydrocortisone NDC 0316-0186
- Generic Name
- Hydrocortisone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydrocortisone NDC 0316-0193
- Generic Name
- Hydrocortisone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSarna NDC 0316-0230
- Generic Name
- Pramoxine Hydrochloride
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Crown Laboratories, Inc
NDC Product
Human Otc DrugSarna NDC 0316-0234
- Generic Name
- Pramoxine Hydrochloride, Menthol
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC
NDC Product
Human Prescription DrugTriamcinolone Acetonide NDC 0168-0002
- Generic Name
- Triamcinolone Acetonide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTriamcinolone Acetonide NDC 0168-0003
- Generic Name
- Triamcinolone Acetonide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTriamcinolone Acetonide NDC 0168-0004
- Generic Name
- Triamcinolone Acetonide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugKetoconazole NDC 0168-0099
- Generic Name
- Ketoconazole
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTerconazole NDC 0168-0346
- Generic Name
- Terconazole
- Dosage Form
- Cream
- Route
- Vaginal
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTerconazole Vaginal Cream 0.8% NDC 0168-0347
- Generic Name
- Terconazole
- Dosage Form
- Cream
- Route
- Vaginal
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugOxiconazole Nitrate NDC 0168-0358
- Generic Name
- Oxiconazole Nitrate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Ferndale Laboratories, Inc.
NDC Product
Human Otc DrugDermend Moisturizing Anti-itch NDC 0496-0586
- Generic Name
- Pramoxine Hydrochloride
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPrax NDC 0496-0748
- Generic Name
- Pramoxine Hydrochloride
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Galderma Laboratories, L.P.
NDC Product
Human Prescription DrugSoolantra NDC 0299-3823
- Generic Name
- Ivermectin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugCetaphil Sheer Mineral Sunscreen Stick Spf 50 NDC 0299-4108
- Generic Name
- Titanium Dioxide, Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCetaphil Cracked Skin Repair Balm NDC 0299-4115
- Generic Name
- Dimethicone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCetaphil Gentle Clear Clarifying Acne Cleanser NDC 0299-4119
- Generic Name
- Salicylic Acid
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCetaphil Eczema Soothing Moisturizer NDC 0299-4128
- Generic Name
- Colloidal Oatmeal
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCetaphil Baby Eczema Soothing NDC 0299-4140
- Generic Name
- Colloidal Oatmeal
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCetaphil Daily Facial Moisturizer With Suncreen Spf 50 NDC 0299-4930
- Generic Name
- Octinoxate, Octisalate, Octocrylene, Oxybenzone, Titanium Di...
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugTri-luma NDC 0299-5950
- Generic Name
- Fluocinolone Acetonide, Hydroquinone, And Tretinoin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA
Active Listing
Genuine Aloe Virgin Corporation
NDC Product
Human Otc DrugTriderma Baby Stubborn Eczema Itch Relief NDC 10738-069
- Generic Name
- Colloidal Oatmeal
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Genuine Virgin Aloe Corporation
NDC Product
Human Otc DrugTriderma Tea Tree Foot Cream NDC 10738-011
- Generic Name
- Ttm Foot
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTriderma Lipsore Cream NDC 10738-020
- Generic Name
- Calendula Officinalis
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugHealing All-purpose Cream NDC 10738-032
- Generic Name
- Calendula Officinalis
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugTriderma Eczema Fast Healing Face And Body NDC 10738-054
- Generic Name
- Colloidal Oatmeal
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTriderma Ulcer Defense Healing NDC 10738-057
- Generic Name
- Calendula Officinalis
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugTriderma Intense Fast Healing Multi-purpose Cream NDC 10738-060
- Generic Name
- Calendula Officinalis
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugTriderma Psoriasis Control Face And Body Cream NDC 10738-062
- Generic Name
- Salicylic Acid
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTriderma Foot Defense NDC 10738-064
- Generic Name
- Triderma Foot Defense Cream
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTriderma Intense Fast Healing Multi-purpose Cream NDC 10738-090
- Generic Name
- Calendula Officinalis
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugTriderma Eczema Fast Healing Face Body NDC 10738-154
- Generic Name
- E Relief
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTriderma Stubborn Diaper Rash Relief NDC 10738-168
- Generic Name
- Allantoin Cream
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc DrugChapstick 12 Days Of Christmas NDC 0135-2029
- Generic Name
- White Petrolatum
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChapstick Moisturizer Cool Mint NDC 0573-0768
- Generic Name
- Avobenzone, Octinoxate, And White Petrolatum
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChapstick 12 Days Of Christmas NDC 0573-0804
- Generic Name
- White Petrolatum
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChapstick Holiday Classics Kit NDC 0573-0805
- Generic Name
- White Petrolatum
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChapstick Classic Spearmint NDC 0573-1912
- Generic Name
- Petrolatum
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChapstick Supreme Classic Cherry NDC 0573-1921
- Generic Name
- White Petrolatum
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChapstick Moisturizer Cool Mint NDC 0573-1957
- Generic Name
- Avobenzone, Homosalate, Octisalate, Octocrylene, White Petro...
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChapstick Moisturizer Original NDC 0573-1958
- Generic Name
- Avobenzone, Homosalate, Octisalate, Octocrylene, White Petro...
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChapstick Moisturizer Variety Pack NDC 0573-1959
- Generic Name
- Avobenzone, Homosalate, Octisalate, Octocrylene, White Petro...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChapstick NDC 0573-2027
- Generic Name
- Avobenzone, Octinoxate, And White Petrolatum
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChapstick Classic Medicated NDC 0573-2031
- Generic Name
- Camphor, Menthol, Petrolatum
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPreparation H Rapid Relief NDC 0573-2843
- Generic Name
- Glycerin, Lidocaine, Petrolatum, And Phenylephrine Hydrochlo...
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPreparation H Maximum Strength NDC 0573-2868
- Generic Name
- Glycerin, Petrolatum, Phenylephrine Hcl, Pramoxine Hcl
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAdvil Targeted Relief NDC 0573-6555
- Generic Name
- Camphor, Capsaicin, Menthol, Methyl Salicylate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
KAO USA
NDC Product
Human Otc DrugBiore Aqua Rich Uv NDC 10596-195
- Generic Name
- Octocrylene, Octisalate, Avobenzene, Homosalate
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBiore Aqua Rich Uv NDC 10596-197
- Generic Name
- Octocrylene, Octisalate, Avobenzene, Homosalate
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBiore Uv Aqua Rich NDC 10596-198
- Generic Name
- Octocrylene, Octisalate, Avobenzene, Homosalate
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Kao USA Inc.
NDC Product
Human Otc DrugBiore Pore Unclogging Scrub NDC 10596-161
- Generic Name
- Salicylic Acid
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Avobenzone, Octisalate, Octocrylene
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Avobenzone,octisalate, Octocrylene
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
L. Perrigo Company
NDC Product
Human Otc DrugGood Sense Lansoprazole NDC 0113-0116
- Generic Name
- Lansoprazole
- Dosage Form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugGood Sense Hair Regrowth Treatment NDC 0113-0294
- Generic Name
- Minoxidil
- Dosage Form
- Aerosol, Foam
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Omeprazole NDC 0113-0520
- Generic Name
- Omeprazole
- Dosage Form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugGood Sense Itch Relief NDC 0113-0622
- Generic Name
- Diphenhydramine Hydrochloride, Zinc Acetate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Hemorrhoidal Maximum Strength Pain Relief NDC 0113-0944
- Generic Name
- Glycerin, Phenylephrine Hcl, Pramoxine Hcl, White Petrolatum
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Hair Regrowth Treatment NDC 0113-1129
- Generic Name
- Minoxidil
- Dosage Form
- Aerosol, Foam
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Lice Killing Creme Rinse NDC 0113-1910
- Generic Name
- Permethrin
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMinoxidil NDC 0113-5129
- Generic Name
- Minoxidil
- Dosage Form
- Aerosol, Foam
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Hair Regrowth Treatment NDC 0113-7080
- Generic Name
- Minoxidil
- Dosage Form
- Aerosol, Foam
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Miconazole 3 NDC 0113-7110
- Generic Name
- Miconazole Nitrate
- Dosage Form
- Cream
- Route
- Vaginal
- Marketing
- ANDA
Active Listing
Marnel Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugCrotan NDC 0682-0051
- Generic Name
- Crotamiton
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- ANDA
Active Listing
Medical Products Laboratories, Inc.
NDC Product
Human Otc DrugTopicale NDC 10733-162
- Generic Name
- Benzocaine
- Dosage Form
- Ointment
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Mericon Industries
NDC Product
Human Otc DrugHydrocortisone NDC 0394-0859
- Generic Name
- Hydrocortisone
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Mission Pharmacal Company
NDC Product
Human Prescription DrugAvar-e Green NDC 0178-0460
- Generic Name
- Sulfacetamide Sodium, Sulfur
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugAvar-e Ls NDC 0178-0465
- Generic Name
- Sulfacetamide Sodium, Sulfur
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugAvar-e NDC 0178-0470
- Generic Name
- Sulfacetamide Sodium, Sulfur
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugAvar Ls NDC 0178-0475
- Generic Name
- Sulfacetamide Sodium, Sulfur
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugAvar NDC 0178-0480
- Generic Name
- Sulfacetamide Sodium, Sulfur
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugOvace Plus NDC 0178-0490
- Generic Name
- Sulfacetamide Sodium
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugOvaceplus Plus NDC 0178-0495
- Generic Name
- Sulfacetamide Sodium
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugOvace Plus NDC 0178-0620
- Generic Name
- Sulfacetamide Sodium
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Mylan Pharmaceuticals Inc.
NDC Product
Human Prescription DrugHalcinonide NDC 0378-8056
- Generic Name
- Halcinonide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDoxepin Hydrochloride NDC 0378-8117
- Generic Name
- Doxepin Hydrochloride
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugZonalon NDC 0378-8123
- Generic Name
- Doxepin Hydrochloride
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPrudoxin NDC 0378-8130
- Generic Name
- Doxepin Hydrochloride
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugOmeprazole NDC 0615-8079
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Person and Covey
NDC Product
Human Otc DrugSolbar Zinc Spf38 NDC 0096-0688
- Generic Name
- Solbar Zinc Spf38
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSolbar Sunscreen 40 Zinc NDC 0096-0691
- Generic Name
- Sunscreen
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSolbar Sunscreen 50 Fifty NDC 0096-0693
- Generic Name
- Sunscreen
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAquanil Hc NDC 0096-0732
- Generic Name
- Hydrocortisone
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSolbar Fifty Spf50 NDC 0096-0741
- Generic Name
- Solbar Fifty Spf50
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAquanil Hc NDC 0096-0810
- Generic Name
- Hydrocortisone
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
RUGBY LABORATORIES
NDC Product
Human Otc Drug4 Lidocaine Topical Anesthetic NDC 0536-1267
- Generic Name
- Lidocaine
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRugby Anti-itch NDC 0536-1268
- Generic Name
- Camphor, Menthol
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rugby
NDC Product
Human Otc DrugHemorrhoidal NDC 0536-1288
- Generic Name
- Mineral Oil, Petrolatum, Phenylephrine Hci
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rugby Laboratories
NDC Product
Human Otc DrugRugby Arthritis Pain Relieving Topical Analgesic NDC 0536-1118
- Generic Name
- Capsaicin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRugby Benzoyl Peroxide Wash Acne Medication NDC 0536-1259
- Generic Name
- Benzoyl Peroxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRugby Benzoyl Peroxide Wash Acne Medication NDC 0536-1261
- Generic Name
- Benzoyl Peroxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRugby Muscle Rub Cream NDC 0536-1349
- Generic Name
- Muscle Rub Cream
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugHydrocortisone Cream With Aloe NDC 0536-1407
- Generic Name
- Hydrocortisone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Sandoz Inc
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 0781-1831
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 0781-1852
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 0781-1874
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 0781-6102
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 0781-6104
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sun Pharmaceutical Industries, Inc.
NDC Product
Human Prescription DrugHalog NDC 10631-094
- Generic Name
- Halcinonide Cream
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugProctosol-hc NDC 10631-407
- Generic Name
- Hydrocortisone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugFluocinonide NDC 0093-0262
- Generic Name
- Fluocinonide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluocinonide NDC 0093-0263
- Generic Name
- Fluocinonide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluocinonide NDC 0093-0264
- Generic Name
- Fluocinonide
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImiquimod NDC 0093-3133
- Generic Name
- Imiquimod
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugKetoconazole NDC 0093-3219
- Generic Name
- Ketoconazole
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDoxepin Hydrochloride NDC 0093-9609
- Generic Name
- Doxepin Hydrochloride
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
Trividia Manufacturing Solutions, Inc
NDC Product
Human Otc DrugSelan Plus Zinc Oxide NDC 0159-2200
- Generic Name
- Selan Plus Zinc Oxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Ultraceuticals Pty Ltd
NDC Product
Human Otc Drug- Generic Name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Viatris Specialty LLC
NDC Product
Human Prescription DrugProctofoam Hc NDC 0037-6822
- Generic Name
- Pramoxine Hydrochloride Hydrocortisone Acetate
- Dosage Form
- Aerosol, Foam
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugProctofoam Ns NDC 0037-6823
- Generic Name
- Pramoxine Hydrochloride
- Dosage Form
- Aerosol, Foam
- Route
- Rectal
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugEpifoam NDC 0037-6824
- Generic Name
- Pramoxine Hydrochloride And Hydrocortisone Acetate
- Dosage Form
- Aerosol, Foam
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCortifoam NDC 0037-6830
- Generic Name
- Hydrocortisone Acetate
- Dosage Form
- Aerosol, Foam
- Route
- Topical
- Marketing
- NDA
Active Listing
WALGREEN COMPANY
NDC Product
Human Otc DrugWalgreens 3 Step Acne System NDC 0363-0153
- Generic Name
- Benzoyl Peroxide
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugWalgreens 100 Sheer Broad Spectrum Spf 100 NDC 0363-0228
- Generic Name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugWalgreens Eczema NDC 0363-0258
- Generic Name
- Colloidal Oatmeal
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugWalgreens Acne Control Gel NDC 0363-0269
- Generic Name
- Salicylic Acid
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugWalgreens Apricot Scrub Acne Treatment NDC 0363-0951
- Generic Name
- Salicylic Acid
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerbinafine Hydrochloride NDC 0363-4502
- Generic Name
- Terbinafine Hydrochloride
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMiconazole 3 Walgreen Company NDC 0363-5203
- Generic Name
- Miconazole Nitrate
- Dosage Form
- Kit
- Route
- Vaginal
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugMiconazole 1 Walgreens NDC 0363-5211
- Generic Name
- Miconazole Nitrate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
Walgreen
NDC Product
Human Otc DrugDaily Moisturizer NDC 0363-5990
- Generic Name
- Lotion
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSkin Relief NDC 0363-5995
- Generic Name
- Lotion
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreen Co.
NDC Product
Human Otc DrugDaily Moisturizing NDC 0363-0619
- Generic Name
- Daily Moistruizing
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBaby Eczema Therapy NDC 0363-0986
- Generic Name
- Colloidal Oatmeal
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreen Company
NDC Product
Human Otc DrugWell At Walgreens Blemish And Blackhead Control Apricot NDC 0363-0830
- Generic Name
- Salicylic Acid
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH FINAL
Active Listing
NDC Product
Human Otc DrugWalgreens Tolnaftate NDC 0363-1298
- Generic Name
- Tolnaftate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLansoprazole NDC 0363-1419
- Generic Name
- Lansoprazole
- Dosage Form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugOmeprazole NDC 0363-1819
- Generic Name
- Omeprazole
- Dosage Form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugHydrocortisone NDC 0363-1973
- Generic Name
- Hydrocortisone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMiconazole 3 NDC 0363-2070
- Generic Name
- Miconazole Nitrate
- Dosage Form
- Cream
- Route
- Vaginal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugWalgreens Athletes Foot NDC 0363-2080
- Generic Name
- Terbinafine Hydrochloride
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAthletes Foot NDC 0363-2100
- Generic Name
- Butenafine Hydrochloride
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugJock Itch NDC 0363-2101
- Generic Name
- Butenafine Hydrochloride
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugWalgreens Everyday Clean Dandruff Anti-dandruff NDC 0363-2606
- Generic Name
- Pyrithione Zinc
- Dosage Form
- Shampoo
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugWalgreens Pain Relieving Plus Turmeric Analgesic NDC 0363-3630
- Generic Name
- Trolamine Salicylate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugWalgreens Dandruff Itchy Dry Scalp Defense Anti-dandruff NDC 0363-4138
- Generic Name
- Pyrithione Zinc
- Dosage Form
- Shampoo
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugIvermectin NDC 0363-4230
- Generic Name
- Ivermectin
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Pyrithione Zinc
- Dosage Form
- Shampoo
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugWalgreens Dandruff Plus Conditioner 2 In 1 Anti-dandruff NDC 0363-4673
- Generic Name
- Pyrithione Zinc
- Dosage Form
- Shampoo
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugWalgreens Eczema Relief Body Skin Protectant NDC 0363-8395
- Generic Name
- Oatmeal
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMinoxidil (for Men) NDC 0363-9090
- Generic Name
- Minoxidil
- Dosage Form
- Aerosol, Foam
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMinoxidil (for Women) NDC 0363-9091
- Generic Name
- Minoxidil
- Dosage Form
- Aerosol, Foam
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugWalgreens Pain Relieving Foot Pain Relief NDC 0363-9379
- Generic Name
- Apis Mellifera, Gelsemium Sempervirens Whole, And Pseudognap...
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugWalgreens Clinical Strength Medicated Dandruff Anti-dandruff, Anti-seborrheic Dermatitis NDC 0363-9422
- Generic Name
- Selenium Sulfide
- Dosage Form
- Shampoo
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreens
NDC Product
Human Otc DrugWalgreens Hemorrhoidal Pain Relief NDC 0363-1217
- Generic Name
- Glycerin 14.4%, Lidocaine 5%, Petrolatum 15%, Phenylephrine ...
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPain And Itch Relief 4% Lidocaine NDC 0363-3001
- Generic Name
- Lidocaine
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugWalgreen Anti Itch NDC 0363-4262
- Generic Name
- Camphor, Menthol
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugDaily Moisturizer NDC 0363-5934
- Generic Name
- Lotion
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreens Co.
NDC Product
Human Otc DrugHydrocortisone NDC 0363-1333
- Generic Name
- Hydrocortisone
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreens Company
NDC Product
Human Otc DrugAnti-itch Medicated Maximum Strength NDC 0363-2311
- Generic Name
- Benzocaine And Resorcinol
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugWalgreens Anti Itch Cream NDC 0363-2315
- Generic Name
- Anti Itch Cream
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
NDC Product
Human Prescription DrugPremarin Vaginal NDC 0046-0872
- Generic Name
- Conjugated Estrogens
- Dosage Form
- Cream
- Route
- Vaginal
- Marketing
- NDA
Active Listing
