NDC Product
Human Otc DrugPetroleum NDC 10202-069
- Generic Name
- White Petrolatum
- Dosage Form
- Jelly
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Butylated Hydroxytoluene, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 1P9D0Z171K.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 128-37-0 and the RxNorm Concept ID (RxCUI) 1848. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
BUTYLATED HYDROXYTOLUENE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
1P9D0Z171K
The specific atomic composition represented as a molecular structure string.
InChIKey
C15H24O International Chemical Identifier digital signature for unique molecular identification.
SMILES String
NLZUEZXRPGMBCV-UHFFFAOYSA-N Line notation for describing the chemical structure and connectivity of atoms.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
Cc1cc(c(O)c(c1)C(C)(C)C)C(C)(C)C
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Butylated Hydroxytoluene. 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
BHT
OF
Common Names & Synonyms
2,6-DI-TERT-BUTYL-P-CRESOL
CN
2,6-DITERTIARY-BUTYL-P-CRESOL
CN
4-METHYL-2,6-DITERTIARY-BUTYL-PHENOL
CN
BHT [FCC]
CN
BUTYLATED HYDROXYTOLUENE
CN
BUTYLATED HYDROXYTOLUENE (E 321)
CN
BUTYLATED HYDROXYTOLUENE [FHFI]
CN
BUTYLATED HYDROXYTOLUENE [HSDB]
CN
BUTYLATED HYDROXYTOLUENE [IARC]
CN
BUTYLATED HYDROXYTOLUENE [II]
CN
BUTYLATED HYDROXYTOLUENE [MART.]
CN
BUTYLATED HYDROXYTOLUENE [MI]
CN
BUTYLATED HYDROXYTOLUENE [NF]
CN
BUTYLATED HYDROXYTOLUENE [USP-RS]
CN
BUTYLATED HYDROXYTOLUENE [VANDF]
CN
BUTYLATED HYDROXYTOLUENE [WHO-DD]
CN
BUTYLATED HYDROXYTOLUENE [WHO-IP]
CN
BUTYLHYDROXYTOLUENE [EP MONOGRAPH]
CN
BUTYLHYDROXYTOLUENUM [WHO-IP LATIN]
CN
KERABIT
CN
Systematic Nomenclature
2,6-BIS(1,1-DIMETHYLETHYL)-4-METHYLPHENOL
SYS
2,6-DI-TERT-BUTYL-P-CRESOL2,6-BIS(1,1-DIMETHYLETHYL)-4-METHYL-PHENOL
SYS
BUTYLHYDROXYTOLUENE
SYS
PHENOL, 2,6-BIS(1,1-DIMETHYLETHYL)-4-METHYL-
SYS
Technical Codes
E-321
CD
FEMA NO. 2184
CD
INS NO.321
CD
INS-321
CD
NSC-6347
CD
NDC Products Containing BUTYLATED HYDROXYTOLUENE
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
7-Select
Active Listing
Access Business Group LLC
NDC Product
Human Otc DrugArtistry Skin Nutrition Balancing Matte Day NDC 10056-040
- Generic Name
- Avobenzone, Octisalate, Octocrylene
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugArtistry Skin Nutrition Hydrating Day NDC 10056-041
- 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
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugArtistry Skin Nutrition Renewing Reactivation Day Spf 30 NDC 10056-051
- Generic Name
- Avobenzone, Octisalate, Octocrylene
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Salicylic Acid
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Acme United Corporation
NDC Product
Human Otc DrugFirst Aid Only First Aid/burn NDC 0924-5011
- Generic Name
- Lidocaine Hydrochloride And Benzalkonium Chloride
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFirst Aid Only First Aid/burn NDC 0924-5730
- Generic Name
- Lidocaine Hydrochloride, Benzalkonium Chloride
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Actavis Pharma, Inc.
NDC Product
Human Prescription DrugClindamycin Phosphate And Tretinoin NDC 0472-1790
- Generic Name
- Clindamycin Phosphate And Tretinoin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- ANDA
Active Listing
Allergan, Inc.
NDC Product
Human Otc DrugRefresh Optive Mega-3 Pf NDC 0023-3988
- Generic Name
- Carboxymethylcellulose Sodium, Glycerin, Polysorbate 80
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRefresh Optive Mega-3 NDC 0023-5773
- Generic Name
- Carboxymethylcellulose Sodium, Glycerin And Polysorbate 80
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Astellas Pharma US, Inc.
NDC Product
Human Prescription DrugMyrbetriq NDC 0469-2601
- Generic Name
- Mirabegron
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMyrbetriq NDC 0469-2602
- Generic Name
- Mirabegron
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMyrbetriq NDC 0469-5020
- Generic Name
- Mirabegron
- Dosage Form
- Granule, For Suspension, Extended Release
- Route
- Oral
- Marketing
- NDA
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
NDC Product
Human Prescription DrugRenova NDC 0187-5150
- Generic Name
- Tretinoin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugJublia NDC 0187-5400
- Generic Name
- Efinaconazole
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- NDA
Active Listing
Bausch Health US, LLC
NDC Product
Human Prescription DrugAltreno NDC 0187-0005
- Generic Name
- Tretinoin
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- NDA
Active Listing
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
NDC Product
Human Prescription DrugTargretin NDC 0187-5525
- Generic Name
- Bexarotene
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- NDA
Active Listing
Bayer HealthCare LLC
NDC Product
Human Otc DrugTinactin Jock Itch NDC 11523-0138
- Generic Name
- Tolnaftate
- Dosage Form
- Aerosol, Powder
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTinactin NDC 11523-0165
- Generic Name
- Tolnaftate
- Dosage Form
- Aerosol, Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Bayer HealthCare LLC.
NDC Product
Human Otc DrugAlka-seltzer Cool Action Heartburn Relief Mint NDC 0280-0001
- Generic Name
- Calcium Carbonate
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlka-seltzer Heartburn Relief Peppermint NDC 0280-0002
- Generic Name
- Calcium Carbonate
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLotrimin Daily Prevention Deo NDC 11523-0010
- Generic Name
- Tolnaftate
- Dosage Form
- Aerosol, Powder
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLotrimin Daily Prevent Deodorant NDC 11523-0136
- Generic Name
- Tolnaftate
- Dosage Form
- Aerosol, Powder
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTinactin Deodorant NDC 11523-0137
- Generic Name
- Tolnaftate
- Dosage Form
- Aerosol, Powder
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTinactin NDC 11523-0139
- Generic Name
- Tolnaftate
- Dosage Form
- Aerosol, Powder
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTinactin Antifungal NDC 11523-4162
- Generic Name
- Tolnaftate
- Dosage Form
- Aerosol, Powder
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Beiersdorf Inc
NDC Product
Human Otc DrugAquaphor Lip Protectant And Sunscreen NDC 10356-111
- Generic Name
- Petrolatum, Avobenzone, Octinoxate, Octisalate, Octocrylene,...
- Dosage Form
- Lotion
- 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 DrugNivea Smoothness Lip Care NDC 10356-819
- Generic Name
- Avobenzone,octocrylene
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Cosette Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugFluocinolone Acetonide NDC 0713-0709
- Generic Name
- Fluocinolone Acetonide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTazarotene NDC 0713-0804
- Generic Name
- Tazarotene
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTazarotene NDC 0713-0805
- Generic Name
- Tazarotene
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- ANDA
Active Listing
ESTEE LAUDER INC
NDC Product
Human Otc DrugDaywear Multi-protection Antii-oxidant 24h-moisture Creme Broad Spectrum Spf 15 Normal/combination Skin NDC 11559-049
- Generic Name
- Avobenzone And Octisalate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Avobenzone, Octisalate, And Octocrylene
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugResilience Multi-effect Tri-peptide Face And Neck Creme Broad Spectrum Spf 15 Dry Skin NDC 11559-053
- Generic Name
- Avobenzone, Octisalate, And Octocrylene
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Avobenzone, Homosalate, Octisalate, And Octocrylene
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Avobenzone, Octisalate, And Octocrylene
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
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
NDC Product
Human Otc Drug- Generic Name
- Ensulizole, Octinoxate, Octisalate, And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Avobenzone, Homosalate, Octisalate, Octocrylene, And Oxybenz...
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Octinoxate And Titanium Dioxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Octinoxate, Titanium Dioxide And Zinc Oxide
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFuturist Skin Tint Serum NDC 11559-063
- Generic Name
- Octinoxate,octisalate,zinc Oxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugDaywear Advanced Multi-protection Anti-oxidant 24h-moisture Creme Broad Spectrum Spf15 NDC 11559-064
- Generic Name
- Avobenzone, Homosalate, Octisalate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Avobenzone,homosalate,octisalate, And Octocrylene
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Endo USA, Inc.
NDC Product
Human Prescription DrugDutasteride And Tamsulosin Hydrochloride NDC 10370-280
- Generic Name
- Dutasteride And Tamsulosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
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
Galderma Laboratories, L.P.
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 Prescription DrugTri-luma NDC 0299-5950
- Generic Name
- Fluocinolone Acetonide, Hydroquinone, And Tretinoin
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc DrugChildrens Advil NDC 0573-0170
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugChildrens Advil NDC 0573-0171
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugInfants Advil NDC 0573-0191
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension/ Drops
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugChildrens Advil NDC 0573-0207
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugChildrens Advil NDC 0573-0232
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugChildrens Advil NDC 0573-0290
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- NDA
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
Hikma Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugCalcitriol NDC 0054-0007
- Generic Name
- Calcitriol
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEverolimus NDC 0054-0470
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEverolimus NDC 0054-0471
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEverolimus NDC 0054-0472
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEverolimus NDC 0054-0480
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEverolimus NDC 0054-0481
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEverolimus NDC 0054-0497
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIndomethacin NDC 0054-1950
- Generic Name
- Indomethacin
- Dosage Form
- Suppository
- Route
- Rectal
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCalcitriol NDC 0054-3120
- Generic Name
- Calcitriol
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Kao USA Inc.
NDC Product
Human Otc DrugBiore Blemish Fighting Ice Cleanser NDC 10596-159
- Generic Name
- Salicylic Acid
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBiore Witch Hazel Pore Clarifying Cleanser NDC 10596-188
- Generic Name
- Salicylic Acid
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBan Roll-on Antiperspirant Deodorant Regular NDC 10596-336
- Generic Name
- Aluminum Chlorohydrate
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
L. Perrigo Company
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 All Day Allergy NDC 0113-0981
- Generic Name
- Cetirizine Hydrochloride
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- ANDA
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 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
Lannett Company, Inc.
NDC Product
Human Prescription DrugDronabinol NDC 0527-4125
- Generic Name
- Dronabinol
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Major Pharmaceuticals
NDC Product
Human Prescription DrugDabigatran Etexilate NDC 0904-7253
- Generic Name
- Dabigatran Etexilate
- Dosage Form
- Capsule, Coated Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDabigatran Etexilate NDC 0904-7254
- Generic Name
- Dabigatran Etexilate
- Dosage Form
- Capsule, Coated Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDabigatran Etexilate NDC 0904-7255
- Generic Name
- Dabigatran Etexilate
- Dosage Form
- Capsule, Coated Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
Merck Sharp & Dohme LLC
NDC Product
Human Prescription DrugIsentress NDC 0006-0227
- Generic Name
- Raltegravir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIsentress NDC 0006-0473
- Generic Name
- Raltegravir
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIsentress NDC 0006-0477
- Generic Name
- Raltegravir
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIsentress NDC 0006-3080
- Generic Name
- Raltegravir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIsentress NDC 0006-3603
- Generic Name
- Raltegravir
- Dosage Form
- Granule, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
Mylan Pharmaceuticals Inc.
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
NDC Product
Human Prescription DrugTretinoin NDC 0378-8090
- Generic Name
- Tretinoin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- ANDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugEscitalopram NDC 0615-8475
- Generic Name
- Escitalopram Oxalate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEscitalopram NDC 0615-8476
- Generic Name
- Escitalopram Oxalate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEscitalopram NDC 0615-8477
- Generic Name
- Escitalopram Oxalate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Nice-Pak Products, LLC
NDC Product
Human Otc DrugPetroleum Skin Protectant NDC 11344-069
- Generic Name
- White Petrolatum
- Dosage Form
- Jelly
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Novartis Pharmaceuticals Corporation
NDC Product
Human Prescription DrugZortress NDC 0078-0414
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZortress NDC 0078-0415
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZortress NDC 0078-0417
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAfinitor NDC 0078-0566
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAfinitor NDC 0078-0567
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAfinitor NDC 0078-0594
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAfinitor NDC 0078-0620
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAfinitor Disperz NDC 0078-0626
- Generic Name
- Everolimus
- Dosage Form
- Tablet, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAfinitor Disperz NDC 0078-0627
- Generic Name
- Everolimus
- Dosage Form
- Tablet, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAfinitor Disperz NDC 0078-0628
- Generic Name
- Everolimus
- Dosage Form
- Tablet, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
Padagis US LLC
NDC Product
Human Prescription DrugPodofilox NDC 0574-0621
- Generic Name
- Podofilox
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- ANDA
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
NDC Product
Human Prescription DrugTretinoin NDC 0574-2301
- Generic Name
- Tretinoin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTretinoin NDC 0574-2325
- Generic Name
- Tretinoin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0574-7110
- Generic Name
- Morphine Sulfate
- Dosage Form
- Suppository
- Route
- Rectal
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0574-7112
- Generic Name
- Morphine Sulfate
- Dosage Form
- Suppository
- Route
- Rectal
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0574-7114
- Generic Name
- Morphine Sulfate
- Dosage Form
- Suppository
- Route
- Rectal
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0574-7116
- Generic Name
- Morphine Sulfate
- Dosage Form
- Suppository
- Route
- Rectal
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugVyndamax NDC 0069-8730
- Generic Name
- Tafamidis
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
Port Jervis Laboratories, Inc
NDC Product
Human Otc Drug- Generic Name
- Avobenzone, Homosalate, Octisalate, And Octocrylene
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
REVLON
NDC Product
Human Otc DrugCeramide Lift And Firm NDC 10967-666
- Generic Name
- Octinoxate, Oxybenzone, Avobenzone, Octisalate, Octocrylene
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCeramide Lift And Firm Eye Spf 15 NDC 10967-667
- Generic Name
- Oxybenzone, Octinoxate
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCeramide Makeup Spf 15 NDC 10967-668
- Generic Name
- Octinoxate, Titanium Dioxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEight Hour Nourishing Lip Spf 20 NDC 10967-671
- Generic Name
- Octinoxate, Avobenzone
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEa Eight Hour Skin Protectant NDC 10967-672
- Generic Name
- Petrolatum
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEight Hour Skin Fragrance Free NDC 10967-673
- Generic Name
- Petrolatum
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEa Eight Hr Lip Sheer Tints NDC 10967-674
- Generic Name
- Oxybenzone, Padimate O, Petrolatum
- Dosage Form
- Lipstick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFlawless Future Spf 30 NDC 10967-683
- Generic Name
- Octinoxate, Octisalate, Oxybenzone, Avaobenzone
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEight Hour Lip Protectant Spf 15 NDC 10967-692
- Generic Name
- Petrolatum, Oxybenzone, Octinoxate, Avobenzone
- Dosage Form
- Lipstick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
REVLON CONSUMER PRODUCTS CORP
NDC Product
Human Otc DrugElizabeth Arden Eight Hr Protectant Clear NDC 10967-676
- Generic Name
- Lip Protectant
- Dosage Form
- Lipstick
- 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
NDC Product
Human Otc DrugPrevage Anti Aging Spf 30 NDC 10967-686
- Generic Name
- Octisalate, Octinoxate, Oxybenzone, Avobenzone, Octocrylene,
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Revlon Consumer Products Corp
NDC Product
Human Otc DrugPrevage Anti-aging Moisture Cream NDC 10967-688
- Generic Name
- Octinoxate, Octisalate, Oxybenzone, Octocrylene, Avobenzone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Revlon Consumer Products Corp.
NDC Product
Human Otc DrugMitchum Clinical Soft Solid Powder Fresh NDC 10967-678
- Generic Name
- Aluminum Zirconium Tetrachlorohydrex Gly 20.0%
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMitchum Clinical Soft Solid Pure Fresh NDC 10967-680
- Generic Name
- Aluminum Zirconium Tetrachlorohydrex Gly 20.0%
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMitchum Clinical Soft Solid Unscented NDC 10967-681
- Generic Name
- Aluminum Zirconium Tetrachlorohydrex Gly 20.0%
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMitchum Clinical Soft Solid Clean Control NDC 10967-682
- Generic Name
- Aluminum Zirconium Tetrachlorohydrex Gly 20.0%
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMitchum Clinical Soft Solid Sport NDC 10967-785
- Generic Name
- Aluminum Zirconium Tetrachlorohydrex Gly 20.0%
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Antiperspirant And Deodorant
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Antiperspirant And Deodorant
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Antiperspirant And Deodorant
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Antiperspirant And Deodorant
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rugby Laboratories
NDC Product
Human Otc DrugRugby Lidocaine NDC 0536-1357
- Generic Name
- Lidocaine 4%
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Original Flavor NDC 0536-3029
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Original Flavor NDC 0536-3030
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine Polacrilex NDC 0536-3404
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine Polacrilex NDC 0536-3405
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
SC Johnson Professional USA, Inc.
NDC Product
Human Otc DrugStokoderm Sunscreen Pure NDC 11084-032
- Generic Name
- Avobenzone, Octocrylene, Octisalate, And Homosalate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
SMASHBOX BEAUTY COSMETICS, INC
NDC Product
Human Otc Drug- Generic Name
- Octinoxate, Titanium Dioxide, And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
TARGET CORPORATION
NDC Product
Human Otc DrugChewable Low Dose Aspirin NDC 11673-493
- Generic Name
- Aspirin
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
TARGET Corporation
NDC Product
Human Otc DrugMiconazole 7 NDC 11673-049
- Generic Name
- Miconazole Nitrate
- Dosage Form
- Cream
- Route
- Vaginal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMinoxidil (for Men) NDC 11673-157
- Generic Name
- Minoxidil
- Dosage Form
- Aerosol, Foam
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMinoxidil (for Women) NDC 11673-158
- Generic Name
- Minoxidil
- Dosage Form
- Aerosol, Foam
- Route
- Topical
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugFidaxomicin NDC 0480-2596
- Generic Name
- Fidaxomicin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
The Mentholatum Company
NDC Product
Human Otc DrugSoftlips Vanilla NDC 10742-3051
- Generic Name
- Dimethicone, Octinoxate, Octisalate, Oxybenzone
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSoftlips Cherry Cordial, Maple Butter, Frosted Berry NDC 10742-7001
- Generic Name
- Dimethicone, Octinoxate, Octisalate, Oxybenzone
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSoftlips Cherry, Raspberry, Vanilla NDC 10742-7002
- Generic Name
- Dimethicone
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSoftlips Watermelon, Tropical Coconut, Peach Passion NDC 10742-7003
- Generic Name
- Dimethicone
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSoftlips Salted Caramel, Candy Apple, Marshmallow Ghost NDC 10742-7004
- Generic Name
- Dimethicone, Octinoxate, Octisalate, Oxybenzone
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSoftlips Tropical Coconut Peach Passion NDC 10742-7005
- Generic Name
- Dimethicone
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSoftlips Peach Passion NDC 10742-7006
- Generic Name
- Dimethicone
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSoftlips Tropical Coconut NDC 10742-7007
- Generic Name
- Dimethicone
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSoftlips Watermelon NDC 10742-7008
- Generic Name
- Dimethicone
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSoftlips Vanilla, Watermelon, Cherry NDC 10742-7009
- Generic Name
- Dimethicone, Octinoxate, Octisalate, Oxybenzone
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Dimethicone, Octinoxate, Octisalate, Oxybenzone
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSoftlips Pearl Plus Vanilla NDC 10742-7011
- Generic Name
- Dimethicone, Octinoxate, Octisalate, Oxybenzone
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSoftlips Raspberry NDC 10742-8470
- Generic Name
- Dimethicone, Octinoxate, Octisalate, Oxybenzone
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSoftlips Watermelon NDC 10742-8476
- Generic Name
- Dimethicone, Octinoxate, Octisalate, Oxybenzone
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSoftlips Vanilla Watermelon NDC 10742-8477
- Generic Name
- Dimethicone, Octinoxate, Octisalate, Oxybenzone
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSoftlips Vanilla Watermelon NDC 10742-8478
- Generic Name
- Dimethicone, Octinoxate, Octisalate, Oxybenzone
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSoftlips Vanilla NDC 10742-8508
- Generic Name
- Dimethicone
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSoftlips Marshmallow Ghost NDC 10742-8510
- Generic Name
- Dimethicone, Octinoxate, Octisalate, Oxybenzone
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSoftlips Cherry NDC 10742-8512
- Generic Name
- Dimethicone, Octinoxate, Octisalate, Oxybenzone
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSoftlips Peppermint NDC 10742-8517
- Generic Name
- Dimethicone, Octinoxate, Octisalate, Oxybenzone
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSoftlips Peppermint Swirl NDC 10742-8518
- Generic Name
- Dimethicone
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSoftlips Pearl NDC 10742-8573
- Generic Name
- Octinoxate, Octisalate
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRed Cross Canker Sore NDC 10742-8915
- Generic Name
- Benzocaine
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Upsher-Smith Laboratories, LLC
NDC Product
Human Prescription DrugTorpenz NDC 0245-0822
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTorpenz NDC 0245-0823
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTorpenz NDC 0245-0824
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTorpenz NDC 0245-0825
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreen Company
NDC Product
Human Otc DrugWalgreens Moisture Barrier NDC 0363-3680
- Generic Name
- Menthol, And Zinc Oxide
- 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
Walgreens
NDC Product
Human Otc DrugWalgreens Athletes Foot NDC 0363-0155
- Generic Name
- Tolnaftate Spray
- Dosage Form
- Aerosol, Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNicotine Polacrilex Original NDC 0363-1608
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine Polacrilex Original NDC 0363-1609
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-3911
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-9290
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-9350
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreens Company
NDC Product
Human Otc DrugTolnaftate NDC 0363-1746
- Generic Name
- Tolnaftate Athletes Foot Powder Spray
- Dosage Form
- Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
