NDC Product
Human Prescription DrugSucralfate NDC 17856-0306
- Generic Name
- Sucralfate
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Sorbic Acid, uniquely identified by the FDA Unique Ingredient Identifier (UNII) X045WJ989B.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 110-44-1 and the RxNorm Concept ID (RxCUI) 1311139. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
SORBIC ACID
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
X045WJ989B
The specific atomic composition represented as a molecular structure string.
InChIKey
C6H8O2 International Chemical Identifier digital signature for unique molecular identification.
SMILES String
WSWCOQWTEOXDQX-MQQKCMAXSA-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
C/C=C/C=C/C(=O)O
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Sorbic Acid. 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
SORBIC ACID
OF
Common Names & Synonyms
(E,E)-2,4-HEXADIENOIC ACID [FHFI]
CN
2,4-HEXADIENOIC ACID, (E,E)-
CN
SORBIC ACID [EP MONOGRAPH]
CN
SORBIC ACID [FCC]
CN
SORBIC ACID [HSDB]
CN
SORBIC ACID [II]
CN
SORBIC ACID [MART.]
CN
SORBIC ACID [MI]
CN
SORBIC ACID [USP-RS]
CN
SORBIC ACID [VANDF]
CN
SORBIC ACID [WHO-DD]
CN
Systematic Nomenclature
(2E,4E)-2,4-HEXADIENOIC ACID
SYS
(E,E)-2,4-HEXADIENOIC ACID
SYS
.ALPHA.-TRANS-.GAMMA.-TRANS-SORBIC ACID
SYS
2-PROPENYLACRYLIC ACID
SYS
Technical Codes
FEMA NO. 3921
CD
INS-200
CD
NSC-35405
CD
NSC-49103
CD
NSC-50268
CD
NDC Products Containing SORBIC ACID
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
ATLANTIC BIOLOGICALS CORP.
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 17856-1133
- Generic Name
- Spironolactone
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions
NDC Product
Human Otc DrugMyco Clinic Pain Relief NDC 24909-010
- Generic Name
- Menthol
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMyco Clinic Pain Relief NDC 24909-012
- Generic Name
- Camphor, Menthol
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMyco Clinic Pain Relief NDC 24909-013
- Generic Name
- Camphor, Menthol
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasilmed Onc NDC 24909-029
- Generic Name
- Allantoin
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil Bruise And Pain Relief Maximum Strength NDC 24909-042
- Generic Name
- Camphor, Menthol
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil Folliculitis Cream Maximum Strength NDC 24909-064
- Generic Name
- Clotrimazole
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Albertsons
NDC Product
Human Otc Drug4x Medicated Gum Cream NDC 21130-621
- Generic Name
- Benzocaine
- Dosage Form
- Cream
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Alchemee, LLC
NDC Product
Human Otc DrugProactivplus Pore Clearing Treatment NDC 11410-047
- Generic Name
- Salicylic Acid
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Allergan, Inc.
NDC Product
Human Otc DrugTotal Defense Repair Broad Spectrum Spf 34 Sunscreen NDC 0023-5494
- Generic Name
- Octinoxate, Octisalate And Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Octinoxate, Octisalate, Titanium Dioxide And Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Zinc Oxide And Octinoxate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugCrinone NDC 0023-6150
- Generic Name
- Progesterone
- Dosage Form
- Gel
- Route
- Vaginal
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCrinone NDC 0023-6151
- Generic Name
- Progesterone
- Dosage Form
- Gel
- Route
- Vaginal
- Marketing
- NDA
Active Listing
Arbor Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugErythromycin NDC 24338-102
- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugErythromycin NDC 24338-104
- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Atlantic Biological Corp.
NDC Product
Human Prescription DrugCyproheptadine Hydrochloride NDC 17856-0504
- Generic Name
- Cyproheptadine Hydrochloride
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- ANDA
Active Listing
BELMORA LLC
NDC Product
Human Otc DrugAnadent Kanka Gel NDC 27854-177
- Generic Name
- Benzocaine
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
BURT'S BEES, INC.
NDC Product
Human Otc DrugNas Max Strength Spot Treatment NDC 26052-022
- Generic Name
- Salicylic Acid
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH FINAL
Active Listing
NDC Product
Human Otc DrugRenewal Firming Day Broad Spectrum Spf 30 NDC 26052-027
- Generic Name
- Titanium Dioxide, Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH FINAL
Active Listing
Bausch & Lomb Incorporated
NDC Product
Human Prescription DrugDiclofenac Sodium NDC 24208-457
- Generic Name
- Diclofenac Sodium
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- ANDA
Active Listing
Bausch Health US LLC
NDC Product
Human Prescription DrugRetin-a Micro NDC 0187-5140
- Generic Name
- Tretinoin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRetin-a Micro NDC 0187-5144
- Generic Name
- Tretinoin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRetin-a Micro NDC 0187-5146
- Generic Name
- Tretinoin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRetin-a Micro NDC 0187-5148
- Generic Name
- Tretinoin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- NDA
Active Listing
Bausch Health US, LLC
NDC Product
Human Prescription DrugRetin-a NDC 0187-5160
- Generic Name
- Tretinoin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRetin-a NDC 0187-5162
- Generic Name
- Tretinoin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRetin-a NDC 0187-5164
- Generic Name
- Tretinoin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRetin-a NDC 0187-5170
- Generic Name
- Tretinoin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRetin-a NDC 0187-5172
- Generic Name
- Tretinoin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- NDA
Active Listing
Bayer HealthCare LLC.
NDC Product
Human Otc DrugAlka-seltzer Extra Strength Heartburn Reliefchews NDC 0280-0042
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlka-seltzer Kids Tummy Reliefchews NDC 0280-0051
- Generic Name
- Calcium Carbonate And Dimethicone
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlka-seltzer Cool Action Extra Strength Reliefchews Mint NDC 0280-0058
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlka-seltzer Heartburn Reliefchews NDC 0280-0221
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlka-seltzer Heartburn Reliefchews Strawberry And Orange NDC 0280-0224
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Calcium Carbonate And Simethicone
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlka-seltzer Ultra Strength Heartburn Reliefchews NDC 0280-0245
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Belmora LLC
NDC Product
Human Otc DrugAnadent Childrens Kanka Gel NDC 27854-178
- Generic Name
- Eugenol
- Dosage Form
- Gel
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
BioActive Nutritional, Inc
NDC Product
Human Otc DrugHepatatox NDC 43857-0543
- Generic Name
- Triticum Aestivum, Chelidonium Majus, Taraxacum Officinale, ...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Blistex Inc
NDC Product
Human Otc DrugDeep Renewal Broad Spectrum NDC 10157-1170
- Generic Name
- Dimethicone, Avobenzone, Homosalate, And Octisalate
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Blistex Inc.
NDC Product
Human Otc DrugBlistex Five Star Lip Protection Broad Spectrum NDC 10157-1171
- Generic Name
- Homosalate, Octisalate, Avobenzone, And Dimethicone
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Boiron
NDC Product
Human Otc DrugArnicare Bruise NDC 0220-9085
- Generic Name
- Arnica Montana
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Burt's Bees
NDC Product
Human Otc DrugBb Broad Spectrum Spf 15 Light NDC 26052-030
- Generic Name
- Zinc Oxide Titanium Dioxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBb Broad Spectrum Spf 15 Medium NDC 26052-032
- Generic Name
- Zinc Oxide Titanium Dioxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugOxcarbazepine NDC 31722-687
- Generic Name
- Oxcarbazepine
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSpironolactone NDC 31722-691
- Generic Name
- Spironolactone
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Church & Dwight Co., Inc.
NDC Product
Human Otc DrugOrajel Rescue Relief Pen NDC 10237-731
- Generic Name
- Oral Pain Reliever
- Dosage Form
- Gel
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugOrajel 2x Medicated Gel NDC 10237-782
- Generic Name
- Oral Pain Reliever
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugOrajel 3x Medicated For All Mouth Sores NDC 10237-783
- Generic Name
- Benzocaine, Menthol, Zinc Chloride
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugOrajel 4x Medicated For Toothache And Gum NDC 10237-787
- Generic Name
- Benzalkonium Chloride, Benzocaine, Menthol, Zinc Chloride
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugOrajel 4x Medicated For Toothache And Gum, Cream NDC 10237-788
- Generic Name
- Benzalkonium Chloride, Benzocaine, Menthol, Zinc Chloride
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugOrajel 4x Medicated Pm For Toothache And Gum NDC 10237-789
- Generic Name
- Benzalkonium Chloride, Benzocaine, Menthol, Zinc Chloride
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugOrajel 3x Medicated For Toothache And Gum NDC 10237-790
- Generic Name
- Benzocaine, Menthol, Zinc Chloride
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugOrajel Gum Pain 3x Medicated NDC 10237-792
- Generic Name
- Benzocaine, Menthol, Zinc Chloride
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Cintas Corporation
NDC Product
Human Otc DrugXpect Eyewash NDC 42961-231
- Generic Name
- Eyewash
- Dosage Form
- Solution
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugDental Relief NDC 42961-810
- Generic Name
- Benzocaine
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Combe Incorporated
NDC Product
Human Otc Drug- Generic Name
- Hydrocortisone Acetate
- Dosage Form
- Cream
- 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 DrugGriseofulvin NDC 0713-0850
- Generic Name
- Griseofulvin
- Dosage Form
- Suspension
- Route
- Oral
- 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 DrugTriderm NDC 0316-0165
- Generic Name
- Triamcinolone Acetonide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTriderm NDC 0316-0170
- Generic Name
- Triamcinolone Acetonide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTriderm NDC 0316-0175
- Generic Name
- Triamcinolone Acetonide
- 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 Prescription DrugNystatin Cream NDC 0316-0221
- Generic Name
- Nystatin Cream
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNystatin And Triamcinolone Acetonide NDC 0316-0223
- Generic Name
- Nystatin And Triamcinolone Acetonide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
Crown Laboratories, Inc.
NDC Product
Human Otc DrugDesenex Antifungal Foot Cream NDC 0316-0255
- Generic Name
- Miconazole Nitrate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPanoxyl Clarifying Exfoliant NDC 0316-0296
- Generic Name
- Salicylic Acid
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPanoxyl Acne Banishing Body (spray) NDC 0316-0297
- Generic Name
- Salicylic Acid
- Dosage Form
- Aerosol, Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
DelCorean, LLC
NDC Product
Human Otc DrugSore Throat 911 NDC 35484-204
- Generic Name
- Potassium Chloride
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugCramp911 NDC 35484-924
- Generic Name
- Magnesium Sulfate, Copper Sulfate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugCramp911 NDC 35484-924
- Generic Name
- Magnesium Sulfate, Copper Sulfate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Deseret Biologicals, Inc.
NDC Product
Human Otc DrugCeleragesic NDC 43742-2243
- Generic Name
- Echinacea (angustifolia), Calendula Officinalis, Hamamelis V...
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Dr. Reddy's Laboratories Inc.
NDC Product
Human Prescription DrugDifluprednate Ophthalmic Emulsion NDC 43598-588
- Generic Name
- Difluprednate Ophthalmic
- Dosage Form
- Emulsion
- Route
- Ophthalmic
- Marketing
- ANDA
Active Listing
EPIC PHARMA, LLC
NDC Product
Human Prescription DrugOxcarbazepine NDC 42806-600
- Generic Name
- Oxcarbazepine
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
ESTEE LAUDER INC
NDC Product
Human Otc DrugRe-nutriv Ultra Radiance Makeup Broad Spectrum Spf 20 NDC 11559-057
- Generic Name
- Octinoxate And Titanium Dioxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Eminence Organic Skin Care
NDC Product
Human Otc DrugEminence Lilikoi Daily Defense Moisturizer Spf 40 Sunscreen NDC 15751-3501
- Generic Name
- Zinc Oxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEminence Bright Skin Moisturizer Spf 40 Sunscreen NDC 15751-3503
- Generic Name
- Zinc Oxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEminence Bright Skin Starter Set Kit NDC 15751-3504
- Generic Name
- Zinc Oxide
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Eminence Organic Skin Care Ltd.
NDC Product
Human Otc DrugAcne Advanced Treatment System NDC 15751-3000
- Generic Name
- Salicylic Acid
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAcne Advanced Cleansing NDC 15751-3010
- Generic Name
- Salicylic Acid
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH FINAL
Active Listing
NDC Product
Human Otc DrugAcne Advanced Clarifying Masque NDC 15751-3020
- Generic Name
- Salicylic Acid
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAcne Advanced Clarifying Hydrator NDC 15751-3030
- Generic Name
- Salicylic Acid
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Encube Ethicals, Inc.
NDC Product
Human Prescription DrugTretinoin NDC 21922-043
- Generic Name
- Tretinoin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTretinoin NDC 21922-079
- Generic Name
- Tretinoin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugHydrocortisone NDC 21922-096
- Generic Name
- Hydrocortisone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugHydrocortisone With Aloe NDC 21922-097
- Generic Name
- Hydrocortisone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Exeltis USA, Inc
NDC Product
Human Prescription DrugVitafol-ob Plus Dha Prenatal Supplement Plus Dha NDC 0642-0076
- Generic Name
- Vitamin A, Ascorbic Acid, Vitamin D, .alpha.-tocopherol, Thi...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Exeltis USA, Inc.
NDC Product
Human Prescription DrugSelect-ob Plus Dha Prenatal Supplement Plus Dha NDC 0642-0075
- Generic Name
- .beta.-carotene, Vitamin A Acetate, Ascorbic Acid, Cholecalc...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- UNAPPROVED DRUG OTHER
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
Genuine Virgin Aloe Corporation
NDC Product
Human Otc DrugTriderma Stubborn Diaper Rash Relief NDC 10738-068
- Generic Name
- Allantoin, Dimethicone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
H.E.B
NDC Product
Human Otc DrugH.e.b Baby NDC 37808-913
- Generic Name
- Spf 50 Sunscreen
- Dosage Form
- Aerosol, Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
HEB
NDC Product
Human Otc Drug4x Medicated Toothache And Gum Cream NDC 37808-116
- Generic Name
- Benzocaine
- Dosage Form
- Cream
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug3x Medicated Mouth Sore Gel NDC 37808-691
- Generic Name
- Benzocaine
- Dosage Form
- Gel
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc DrugGas-x Total Relief Maximum Strength NDC 0067-0118
- Generic Name
- Calcium Carbonate, Simethicone
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGas-x Total Relief Maximum Strength NDC 0067-0119
- Generic Name
- Calcium Carbonate, Simethicone
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites NDC 0135-0183
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Berry Shake NDC 0135-0184
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Tropical Fruit Smoothie NDC 0135-0185
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Raspberry Lemonade NDC 0135-0188
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites NDC 0135-0606
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites NDC 0135-0618
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Peppermint NDC 0135-0623
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites With Gas Relief NDC 0135-0624
- Generic Name
- Calcium Carbonate And Simethicone
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Mixed Fruit NDC 0135-0641
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Orange And Cream Es NDC 0135-0642
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Kroger
NDC Product
Human Otc Drug4x Medicated Toothache And Gum Cream NDC 30142-212
- Generic Name
- Benzocaine
- Dosage Form
- Cream
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Laboratoires Boiron
NDC Product
Human Otc DrugCalendula NDC 0220-1105
- Generic Name
- Calendula Officinalis Flowering Top
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugCalendula NDC 0220-1108
- Generic Name
- Calendula Officinalis Flowering Top
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugCalendula NDC 0220-1109
- Generic Name
- Calendula Officinalis Flowering Top
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugArnicare NDC 0220-9021
- Generic Name
- Arnica Montana
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugArnica Value Pack NDC 0220-9047
- Generic Name
- Arnica Montana
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
MAKEUP ART COSMETICS
NDC Product
Human Otc DrugStudio Fix Fluid Spf 15 Broad Spectrum NDC 40046-0072
- Generic Name
- Octinoxate And Titanium Dioxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugStudio Fix Fluid Broad Spectrum Spf 15 NDC 40046-0082
- Generic Name
- Octinoxate, Titanium Dioxide
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Macleods Pharmaceuticals Limited
NDC Product
Human Prescription DrugOxcarbazepine NDC 33342-259
- Generic Name
- Oxcarbazepine
- Dosage Form
- For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNystatin And Triamcinolone Acetonide NDC 33342-482
- Generic Name
- Nystatin And Triamcinolone Acetonide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
Major Pharmaceuticals
NDC Product
Human Prescription DrugClarithromycin NDC 0904-6872
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Marlex Pharmaceuticals, Inc
NDC Product
Human Prescription DrugOxcarbazepine NDC 10135-798
- Generic Name
- Oxcarbazepine
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Mylan Pharmaceuticals Inc.
NDC Product
Human Prescription DrugDifluprednate NDC 0378-7518
- Generic Name
- Difluprednate
- Dosage Form
- Emulsion
- Route
- Ophthalmic
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTretinoin NDC 0378-8082
- Generic Name
- Tretinoin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugTretinoin NDC 0378-8083
- Generic Name
- Tretinoin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugTretinoin NDC 0378-8084
- Generic Name
- Tretinoin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugTretinoin NDC 0378-8085
- Generic Name
- Tretinoin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugTretinoin NDC 0378-8086
- Generic Name
- Tretinoin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NORTHSTAR RX LLC
NDC Product
Human Prescription DrugTretinoin NDC 16714-249
- Generic Name
- Tretinoin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTretinoin NDC 16714-250
- Generic Name
- Tretinoin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTretinoin NDC 16714-270
- Generic Name
- Tretinoin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
Nantong Health & Beyond Hygienic Products Inc.
NDC Product
Human Otc DrugOral Pain Relief NDC 43473-100
- Generic Name
- Benzocaine
- Dosage Form
- Gel
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMymedic Oral Pain Relief Gel NDC 43473-306
- Generic Name
- Benzocaine
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Novartis Pharmaceuticals Corporation
NDC Product
Human Prescription DrugTrileptal NDC 0078-0357
- Generic Name
- Oxcarbazepine
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
PAI Holdings, LLC dba PAI Pharma
NDC Product
Human Prescription DrugSucralfate NDC 0121-0974
- Generic Name
- Sucralfate
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
PD-Rx Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugClarithromycin NDC 43063-823
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Padagis US LLC
NDC Product
Human Prescription DrugSpironolactone NDC 0574-1133
- Generic Name
- Spironolactone
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugTretinoin NDC 0574-2201
- Generic Name
- Tretinoin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTretinoin NDC 0574-2205
- Generic Name
- Tretinoin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTretinoin NDC 0574-2225
- Generic Name
- Tretinoin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
Patrin Pharma, Inc.
NDC Product
Human Prescription DrugPrenatal Plus Vitamins NDC 39328-106
- Generic Name
- Prenatal With Ferrous Fumarate And Folic Acid
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugCyproheptadine Hydrochloride NDC 39328-544
- Generic Name
- Cyproheptadine Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Peaceful Mountain, Inc.
NDC Product
Human Otc DrugEczema Rescue NDC 43846-0008
- Generic Name
- Carbolicum Acidum, Fagopyrum Esculentum, Hydrastis Canadensi...
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugCold Sore Rescue NDC 43846-0031
- Generic Name
- Borax, Dulcamara, Natrum Muriaticum, Ranunculus Bulbosus, Si...
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugMuscle Ice NDC 43846-0073
- Generic Name
- Phytolacca Decandra, Bellis Perennis, Ledum Palustre, Ruta G...
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugArnica Plus NDC 43846-0075
- Generic Name
- Arnica Montana, Hamamelis Virginiana, Rhus Tox
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugBack, Neck And Sciatic Rescue NDC 43846-0076
- Generic Name
- Phytolacca Decandra, Gnaphalium Polycephalum, Hypericum Perf...
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugJoint And Tendon Rescue NDC 43846-0077
- Generic Name
- Bryonia (alba), Ruta Graveolens, Bellis Perennis, Capsicum A...
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugDerma Pain Plus NDC 43846-0080
- Generic Name
- Croton Tiglium, Natrum Muriaticum, Plantago Major, Rhus Toxi...
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugMuscle Rescue NDC 43846-0083
- Generic Name
- Arnica Montana, Rhus Tox, Phytolacca Decandra, Pulsatilla (v...
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Pharmacia & Upjohn Company LLC
NDC Product
Human Prescription DrugCortef NDC 0009-0012
- Generic Name
- Hydrocortisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMedrol NDC 0009-0020
- Generic Name
- Methylprednisolone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMedrol NDC 0009-0022
- Generic Name
- Methylprednisolone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCortef NDC 0009-0031
- Generic Name
- Hydrocortisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCortef NDC 0009-0044
- Generic Name
- Hydrocortisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMedrol NDC 0009-0056
- Generic Name
- Methylprednisolone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMedrol NDC 0009-0073
- Generic Name
- Methylprednisolone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
Port Jervis Laboratories, Inc.
NDC Product
Human Otc Drug- Generic Name
- Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Revlon
NDC Product
Human Otc DrugPrevage Anti-aging Eye Cream Spf 15 NDC 10967-685
- Generic Name
- Octinoxate, Oxybenzone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Revlon Consumer Products Corp
NDC Product
Human Otc DrugRevlon Photoready Insta-fix Makeup NDC 10967-631
- Generic Name
- Titanium Dioxide, Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rite Aid
NDC Product
Human Otc DrugRite Aid Maximum Strength NDC 11822-0316
- Generic Name
- Benzocaine
- Dosage Form
- Gel, Dentifrice
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNighttime 4x Medicated Cream NDC 11822-6300
- Generic Name
- Benzocaine
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rite Aid Corporation
NDC Product
Human Otc DrugEye Wash NDC 11822-9860
- Generic Name
- Water
- Dosage Form
- Solution
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Safeway
NDC Product
Human Otc DrugAnti Itch NDC 21130-433
- Generic Name
- Hydrocortisone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugHydrocortisone NDC 21130-449
- Generic Name
- Hydrocortisone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Sandoz Inc
NDC Product
Human Prescription DrugDifluprednate Ophthalmic NDC 0781-6000
- Generic Name
- Difluprednate Ophthalmic
- Dosage Form
- Emulsion
- Route
- Ophthalmic
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Sheffield Pharmaceuticals LLC
NDC Product
Human Otc DrugSheffield Pain Relief NDC 11527-062
- Generic Name
- Benzocaine
- Dosage Form
- Gel
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSheffield Advanced Scar Gel NDC 11527-725
- Generic Name
- Advanced Scar Gel
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Sun Pharmaceutical Industries, Inc.
NDC Product
Human Prescription DrugProctosol-hc NDC 10631-407
- Generic Name
- Hydrocortisone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
TARGET Corporation
NDC Product
Human Otc DrugDigestive Relief Regular Strength NDC 11673-372
- Generic Name
- Bismuth Subsalicylate
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
TOPCO ASSOCIATES LLC
NDC Product
Human Otc DrugTopco Topcare Everyday Baby Protection Sun Spf 50 NDC 36800-347
- Generic Name
- Octisalate, Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Target
NDC Product
Human Otc DrugWhitening NDC 11673-385
- Generic Name
- Monofluorophosphate
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Target Corporation
NDC Product
Human Otc DrugTarget Advanced Scar Gel NDC 11673-725
- Generic Name
- Advanced Scar Gel
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugErythromycin NDC 0093-5571
- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugErythromycin NDC 0093-5572
- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
The Procter & Gamble Manufacturing Company
NDC Product
Human Otc DrugPepto-bismol NDC 37000-438
- Generic Name
- Bismuth Subsalicylate
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPepto-bismol Cherry NDC 37000-439
- Generic Name
- Bismuth Subsalicylate
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPepto-bismol Ultra NDC 37000-440
- Generic Name
- Bismuth Subsalicylate
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPepto-bismol Ultra Cherry NDC 37000-441
- Generic Name
- Bismuth Subsalicylate
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPepto Bismol Chews NDC 37000-996
- Generic Name
- Bismuth Subsalicylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
TopCare
NDC Product
Human Otc DrugTopco 4x Medicated Toothache And Gum Gel NDC 36800-624
- Generic Name
- Benzocaine
- Dosage Form
- Gel
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Topco Associates LLC
NDC Product
Human Otc DrugTopcare Oral Pain Relief Maximum Strength NDC 36800-512
- Generic Name
- Benzocaine
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Torrent Pharmaceuticals Limited
NDC Product
Human Prescription DrugNystatin And Triamcinolone Acetonide NDC 13668-610
- Generic Name
- Nystatin And Triamcinolone Acetonide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
Upsher-Smith Laboratories, LLC
NDC Product
Human Prescription DrugDifluprednate NDC 0832-6054
- Generic Name
- Difluprednate
- Dosage Form
- Emulsion
- Route
- Ophthalmic
- Marketing
- ANDA
Active Listing
Walgreens
NDC Product
Human Otc DrugSoothe NDC 0363-0073
- Generic Name
- Bismuth Subsalicylate
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNbe Anbesol NDC 0363-0316
- Generic Name
- Benzocaine
- Dosage Form
- Gel
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug4x Medicated Toothache And Gum Cream NDC 0363-0607
- Generic Name
- Benzocaine
- Dosage Form
- Cream
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugWalgreens Sterile Soothing Eye Wash NDC 0363-0700
- Generic Name
- Purified Water
- Dosage Form
- Liquid
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug3x Medicated Mouth Sore Gel NDC 0363-1605
- Generic Name
- Benzocaine
- Dosage Form
- Gel
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPm Toothache Relief NDC 0363-1623
- Generic Name
- Benzocaine
- Dosage Form
- Paste
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug4x Medicated Toothache And Gum Gel NDC 0363-6008
- Generic Name
- Benzocaine
- Dosage Form
- Gel
- Route
- Oral
- 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 DrugWalgreens Advanced Scar Gel NDC 0363-2312
- Generic Name
- Advanced Scar Gel
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
