NDC Product
Human Prescription DrugOmeprazole NDC 50090-7018
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Acetone, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 1364PS73AF.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 67-64-1 and the RxNorm Concept ID (RxCUI) 178. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
ACETONE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
1364PS73AF
The specific atomic composition represented as a molecular structure string.
InChIKey
C3H6O International Chemical Identifier digital signature for unique molecular identification.
SMILES String
CSCPPACGZOOCGX-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
O=C(C)C
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Acetone. 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
ACETONE
OF
Common Names & Synonyms
ACETONE [EP IMPURITY]
CN
ACETONE [EP MONOGRAPH]
CN
ACETONE [FCC]
CN
ACETONE [FHFI]
CN
ACETONE [HSDB]
CN
ACETONE [MART.]
CN
ACETONE [MI]
CN
ACETONE [USP-RS]
CN
ACETONE [VANDF]
CN
ACETONE [WHO-DD]
CN
ACETYLENE INTERMIX (1 PER CENT) IN NITROGEN IMPURITY A [EP Impurity]
CN
CHLOROBUTANOL IMPURITY B [EP IMPURITY]
CN
DESFLURANE IMPURITY H [EP IMPURITY]
CN
ISOFLURANE IMPURITY F [EP IMPURITY]
CN
PYROACETIC ETHER
CN
TAIMAX
CN
Systematic Nomenclature
.BETA.-KETOPROPANE
SYS
2-PROPANONE
SYS
DIMETHYL KETONE
SYS
DIMETHYLFORMALDEHYDE
SYS
PROPANONE
SYS
Technical Codes
FEMA NO. 3326
CD
NSC-135802
CD
NDC Products Containing ACETONE
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 (193), only Active Listings are currently displayed.
Showing 147 active products
A-S Medication Solutions
Active Listing
NDC Product
Human Prescription DrugOmeprazole NDC 50090-7019
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOmeprazole NDC 50090-7021
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Advantice Health, LLC
NDC Product
Human Otc DrugNew Skin Bandage NDC 16864-440
- Generic Name
- Benzethonium Chloride
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Advantice Health, LLC.
NDC Product
Human Otc DrugNew Skin Bandage NDC 16864-450
- Generic Name
- Benzethonium Chloride
- Dosage Form
- Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
AiPing Pharmaceutical, Inc.
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 11788-037
- Generic Name
- Metformin Hydrochloride Extended-release Tablets
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 11788-038
- Generic Name
- Metformin Hydrochloride Extended-release Tablets
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Amazon.com Services LLC
NDC Product
Human Otc DrugEthyl Rubbing Alcohol NDC 72288-876
- Generic Name
- Ethyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Amerisource Bergen
NDC Product
Human Otc DrugGnp Ethyl Rubbing Alcohol 70 Percent NDC 46122-329
- Generic Name
- Ethyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
AmerisourceBergen Drug Corporation
NDC Product
Human Otc DrugBenzethonium Chloride Plus Dyclonine Hydrochloride NDC 46122-525
- Generic Name
- Liquid Bandage
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Apex Energetics Inc.
NDC Product
Human Otc DrugN02 Petrochem NDC 63479-1402
- Generic Name
- Acetone, Anilinum, Benzinum, Benzopyrene, Carbo Vegetabilis,...
- Dosage Form
- Solution/ Drops
- Route
- Sublingual
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
BioActive Nutritional
NDC Product
Human Otc DrugHousehold Antigens NDC 43857-0537
- Generic Name
- Acetone, Sodium Tripolyphosphate, Propylene Glycol, Benzinum...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
BioActive Nutritional, Inc.
NDC Product
Human Otc DrugPneumotox NDC 43857-0533
- Generic Name
- Triticum Aestivum, Alfalfa, Arnica Montana, Asclepias Tubero...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugEnvirotox NDC 43857-0625
- Generic Name
- Triticum Aestivum, Berberis Vulgaris, Lappa Major, Rhamnus P...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Breckenridge Pharmaceutical, Inc.
NDC Product
Human Prescription DrugEverolimus NDC 51991-821
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEverolimus NDC 51991-822
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEverolimus NDC 51991-823
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEverolimus NDC 51991-824
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Bryant Ranch Prepack
NDC Product
Human Prescription DrugOmeprazole NDC 71335-9744
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
CVS Pharmacy
NDC Product
Human Otc DrugMaximum Strength Antifungal Liquid NDC 51316-898
- Generic Name
- Tolnaftate
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMiconazole Nitrate NDC 59779-097
- Generic Name
- Athletes Foot Spray
- Dosage Form
- Aerosol, Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBenzethonium Chloride Plus Dyclonine Hydrochloride NDC 59779-385
- Generic Name
- Liquid Bandage
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBenzethonium Chloride And Dyclonine Hydrochloride NDC 69842-084
- Generic Name
- Liquid Bandage
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCvs Merthiolate NDC 69842-749
- Generic Name
- Benzalkonium Chloride
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
CVS Pharmacy, Inc.
NDC Product
Human Otc DrugEthyl Rubbing Alcohol NDC 59779-164
- Generic Name
- Ethyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugHydromorphone Hydrochloride NDC 31722-119
- Generic Name
- Hydromorphone Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydromorphone Hydrochloride NDC 31722-120
- Generic Name
- Hydromorphone Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydromorphone Hydrochloride NDC 31722-121
- Generic Name
- Hydromorphone Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydromorphone Hydrochloride NDC 31722-122
- Generic Name
- Hydromorphone Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 31722-229
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 31722-230
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 31722-231
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 31722-232
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 31722-233
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 31722-234
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 31722-235
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 31722-236
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Cardinal Health 107, LLC
NDC Product
Human Prescription DrugOmeprazole NDC 55154-2332
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Cardinal Health, 110 dba Leader
NDC Product
Human Otc DrugEthyl Rubbing Alcohol NDC 70000-0020
- Generic Name
- Ethyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Chain Drug Market Association
NDC Product
Human Otc DrugQuality Choice Merthiolate NDC 63868-493
- Generic Name
- Benzalkonium Chloride
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Chain Drug Marketing Association Inc
NDC Product
Human Otc DrugMaximum Strength Antifungal Liquid NDC 83324-301
- Generic Name
- Tolnaftate
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Chattem, Inc.
NDC Product
Human Otc DrugAllegra-d Allergy And Congestion NDC 41167-4320
- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
Clarion Brands, LLC
NDC Product
Human Otc DrugAbsorbine Jr. Plus NDC 69693-411
- Generic Name
- Menthol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAbsorbine Jr. Plus NDC 69693-424
- Generic Name
- Menthol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
DLC Laboratories, Inc
NDC Product
Human Otc DrugTincture Merthiolate NDC 24286-1532
- Generic Name
- Benzalkonium Chloride
- Dosage Form
- Tincture
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Deseret Biologicals, Inc.
NDC Product
Human Otc DrugEnviroclenz NDC 43742-1571
- Generic Name
- Berberis Vulgaris, Carduus Marianus, Chelidonium Majus, Glyc...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugPetrochemical Detox NDC 43742-1580
- Generic Name
- Chelidonium Majus, Taraxacum Officinale, Trifolium Pratense,...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugPollutox NDC 43742-2095
- Generic Name
- Sulphuricum Acidum, Berberis Vulgaris, Arsenicum Album, Benz...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Dr. Reddy's Laboratories Inc
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride (la) NDC 75907-049
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride (la) NDC 75907-050
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride (la) NDC 75907-051
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride (la) NDC 75907-052
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride (la) NDC 75907-053
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Dr.Reddy's Laboratories Limited
NDC Product
Human Prescription DrugDivalproex Sodium NDC 55111-529
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 55111-530
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 55111-531
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
EPIC PHARMA, LLC
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 42806-405
- Generic Name
- Metformin Hydrochloride Tablets
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 42806-406
- Generic Name
- Metformin Hydrochloride Tablet
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Efficient Laboratories Inc
NDC Product
Human Otc DrugHongo Killer NDC 58593-625
- Generic Name
- Tolnaftate
- Dosage Form
- Aerosol, Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Efficient Laboratories Inc.
NDC Product
Human Otc DrugOngo - Fin NDC 58593-800
- Generic Name
- Tolnaftate
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Energique, Inc.
NDC Product
Human Otc DrugHousehold Antigens NDC 44911-0725
- Generic Name
- Acetone, Sodium Tripolyphosphate, Propylene Glycol, Benzinum...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Eskayef Pharmaceuticals Limited
NDC Product
Human Prescription DrugPaliperidone NDC 72658-1253
- Generic Name
- Paliperidone
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPaliperidone NDC 72658-1254
- Generic Name
- Paliperidone
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPaliperidone NDC 72658-1255
- Generic Name
- Paliperidone
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPaliperidone NDC 72658-1256
- Generic Name
- Paliperidone
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
FSA Store Inc.
NDC Product
Human Otc DrugMaximum Strength Antifungal Liquid NDC 81522-077
- Generic Name
- Tolnaftate
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Family Dollar Services, Inc
NDC Product
Human Otc DrugAntifungal Liquid Continuous NDC 55319-539
- Generic Name
- Miconazole Nitrate
- Dosage Form
- Aerosol, Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Foodhold USA
NDC Product
Human Otc DrugBenzethonium Chloride Plus Dyclonine Hydrochloride NDC 41520-089
- Generic Name
- Liquid Bandage
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
GEISS, DESTIN AND DUNN, INC.
NDC Product
Human Otc DrugMiconazole Nitrate NDC 50804-136
- Generic Name
- Antifungal Miconazole Liquid Continuous Spray
- Dosage Form
- Aerosol, Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Gilead Sciences, Inc.
NDC Product
Human Prescription DrugVosevi NDC 61958-2401
- Generic Name
- Sofosbuvir, Velpatasvir, And Voxilaprevir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
HEB
NDC Product
Human Otc DrugBenzethonium Chloride Plus Dyclonine Hydrochloride NDC 37808-512
- Generic Name
- Liquid Bandage
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Harris Teeter, LLC
NDC Product
Human Otc DrugBenzethonium Chloride Plus Dyclonine Hydrochloride NDC 69256-037
- Generic Name
- Liquid Bandage
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Hudson Health LLC
NDC Product
Human Otc DrugLiquid Antifungal Treatment NDC 72446-012
- Generic Name
- Tolnaftate
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBenzethonium Chloride Plus Dyclonine Hydrochloride NDC 72446-100
- Generic Name
- Liquid Bandage
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Humco Holding Group, Inc.
NDC Product
Human Otc DrugEthyl Rubbing Alcohol NDC 0395-0040
- Generic Name
- Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugHumco Merthiolate NDC 0395-8010
- Generic Name
- Benzalkonium Chloride
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Kroger Co.
NDC Product
Human Otc DrugBenzethonium Chloride Plus Dyclonine Hydrochloride NDC 30142-150
- Generic Name
- Liquid Bandage
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
LEADER/ Cardinal Health 110, Inc.
NDC Product
Human Otc DrugLeader Liquid Bandage NDC 70000-0599
- Generic Name
- Benzethonium Chloride Dyclonine Hydrochloride
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAntifungal Liquid NDC 70000-0745
- Generic Name
- Tolnaftate
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Lydia Co., Ltd.
NDC Product
Human Otc DrugAntiphlamine NDC 72988-0028
- Generic Name
- L-menthol, L-camphor, Methyl Salicylate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Major Pharmaceuticals
NDC Product
Human Prescription DrugOmeprazole NDC 0904-6917
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Masaem Company
NDC Product
Human Otc DrugAntiphlamine NDC 87538-0003
- Generic Name
- L-menthol, L-camphor, Methyl Salicylate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Mayne Pharma
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride (la) NDC 51862-611
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride (la) NDC 51862-612
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Meijer Distribution Inc
NDC Product
Human Otc DrugAntifungal Miconazole Liquid Continuous NDC 79481-0599
- Generic Name
- Miconazole Nitrate
- Dosage Form
- Aerosol, Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLiquid Bandage NDC 79481-0606
- Generic Name
- Benzethonium Chloride Plus Dyclonine Hydrochloride
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMaximum Strength Antifungal Liquid NDC 79481-0660
- Generic Name
- Tolnaftate
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Mylan Pharmaceuticals Inc.
NDC Product
Human Prescription DrugSulfasalazine NDC 59762-0104
- Generic Name
- Sulfasalazine
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Natco Pharma Limited
NDC Product
Human Prescription DrugEverolimus NDC 63850-0058
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEverolimus NDC 63850-0059
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEverolimus NDC 63850-0060
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEverolimus NDC 63850-0061
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Nice-Pak Products, LLC
NDC Product
Human Otc DrugRubbing NDC 0869-0876
- Generic Name
- Ethyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEthyl Alcohol NDC 11344-876
- Generic Name
- Ethyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NuCare Pharmaceuticals,Inc.
NDC Product
Human Prescription DrugLansoprazole NDC 68071-3585
- Generic Name
- Lansoprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Nutritional Specialties, Inc.
NDC Product
Human Otc DrugIndustriox NDC 83027-0048
- Generic Name
- Berberis Vulgaris, Taraxacum Officinale, Ammonium Carbonicum...
- Dosage Form
- Spray
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugTap Water Detox NDC 83027-0093
- Generic Name
- Acetone, Aluminium Metallicum, Antimonium Crudum, Arsenicum ...
- Dosage Form
- Spray
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Perrigo Direct, Inc
NDC Product
Human Otc DrugRubbing NDC 50804-876
- Generic Name
- Ethyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugAzulfidine En-tabs NDC 0013-0102
- Generic Name
- Sulfasalazine
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
Pharma Nobis, LLC
NDC Product
Human Otc DrugMerthiolate NDC 82645-912
- Generic Name
- Benzalkonium Chloride
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEthyl Rubbing Alcohol 70 Percent NDC 82645-926
- Generic Name
- Ethyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Premier Brands of America Inc.
NDC Product
Human Otc DrugLiquid Bandage NDC 56104-502
- Generic Name
- Benzethonium Chloride Plus Dyclonine Hydrochloride
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMiconazole Nitrate NDC 56104-903
- Generic Name
- Antifungal Miconazole Liquid Continuous Spray
- Dosage Form
- Aerosol, Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Premier Brands of America, Inc.
NDC Product
Human Otc DrugPremier Solutions Liquid Bandage NDC 56104-246
- Generic Name
- Benzethonium Chloride Dyclonine Hydrochloride
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Professional Complementary Health Formulas
NDC Product
Human Otc DrugIndustriox 6011 NDC 63083-6011
- Generic Name
- Industriox
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugPerfumox 6028 NDC 63083-6028
- Generic Name
- Perfumox
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Qingdao BAHEAL Pharmaceutical Co., Ltd.
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 70247-018
- Generic Name
- Metformin Hydrochloride Extended-release Tablets
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 70247-019
- Generic Name
- Metformin Hydrochloride Extended-release Tablets
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rising Pharma Holdings, Inc.
NDC Product
Human Prescription DrugLansoprazole, Amoxicillin, Clarithromycin NDC 57237-001
- Generic Name
- Lansoprazole, Amoxicillin, Clarithromycin
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
Rooftop Consumer Health, Inc.
NDC Product
Human Otc Drug- Generic Name
- Tolnaftate
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rooftop Consumer health, inc
NDC Product
Human Otc DrugProclearz Professional Fungal Shield NDC 29784-184
- Generic Name
- Tolnaftate
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
STRATEGIC SOURCING SERVICES LLC
NDC Product
Human Otc DrugEthyl Rubbing Alcohol NDC 70677-0056
- Generic Name
- Ethyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Sato Pharmaceutical Co., Ltd.
NDC Product
Human Otc DrugHi Vetic NDC 49873-050
- Generic Name
- Tolnaftate
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Strategic Sourcing Services LLC
NDC Product
Human Otc DrugEthyl Alcohol NDC 70677-1220
- Generic Name
- Ethyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Stratus Pharamceuticals
NDC Product
Human Otc DrugCastellani Paint NDC 58980-820
- Generic Name
- Phenol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Target Corporation
NDC Product
Human Otc DrugBenzethonium Chloride And Dyclonine Hydrochloride NDC 82442-019
- Generic Name
- Liquid Bandage
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAntifungal Liquid NDC 82442-998
- Generic Name
- Tolnaftate
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
The Podiatree Company
NDC Product
Human Otc DrugFortinia Id NDC 54633-216
- Generic Name
- Phenol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCastellani Paint 1.5% NDC 54633-612
- Generic Name
- Phenol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCastellani Paint 1.5% NDC 54633-712
- Generic Name
- Phenol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
The Red Oil Company Inc
NDC Product
Human Otc DrugRed Oil Pain Relief NDC 70537-986
- Generic Name
- Camphor (synthetic), Menthol, Phenol
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Topco Associates LLC
NDC Product
Human Otc DrugBenzethonium Chloride Plus Dyclonine Hydrochloride NDC 36800-382
- Generic Name
- Liquid Bandage
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Topiderm, Inc.
NDC Product
Human Otc DrugGly-sal 5-2 Pads NDC 51326-038
- Generic Name
- Salicylic Acid
- Dosage Form
- Cloth
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGly-sal 10-2 Pads NDC 51326-039
- Generic Name
- Salicylic Acid
- Dosage Form
- Cloth
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGly-sal 10-2 NDC 51326-712
- Generic Name
- Salicylic Acid
- Dosage Form
- Cloth
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugDr. Zenovia Clear Complexion NDC 51326-801
- Generic Name
- Salicylic Acid
- Dosage Form
- Cloth
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
United Natural Foods, Inc. dba UNFI
NDC Product
Human Otc DrugRubbing NDC 41163-876
- Generic Name
- Ethyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Wal-Mart Stores, Inc.
NDC Product
Human Otc DrugAntifungal Liquid NDC 79903-394
- Generic Name
- Tolnaftate
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLiquid Bandage NDC 79903-485
- Generic Name
- Benzethonium Chloride And Dyclonine Hydrochloride
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreen Co.
NDC Product
Human Otc DrugEthyl Rubbing Alcohol NDC 0363-0876
- Generic Name
- Ethyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreen Company
NDC Product
Human Otc DrugBenzethonium Chloride And Dyclonine Hydrochloride NDC 0363-0210
- Generic Name
- Liquid Bandage
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreens Company
NDC Product
Human Otc DrugMaximum Strength Antifungal Liquid NDC 0363-2026
- Generic Name
- Tolnaftate
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMiconazole Nitrate NDC 0363-4208
- Generic Name
- Athletes Foot Liquid
- Dosage Form
- Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAntifungal Liquid NDC 0363-4471
- Generic Name
- Tolnaftate
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walmart Inc.
NDC Product
Human Otc DrugEthyl Alcohol NDC 79903-283
- Generic Name
- Ethyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
WinCo Foods LLC
NDC Product
Human Otc DrugLiquid Bandage NDC 67091-751
- Generic Name
- Benzethonium Chloride Plus Dyclonine Hydrochloride
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
XLCare Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugHydromorphone Hydrochloride NDC 72865-168
- Generic Name
- Hydromorphone Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydromorphone Hydrochloride NDC 72865-169
- Generic Name
- Hydromorphone Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydromorphone Hydrochloride NDC 72865-170
- Generic Name
- Hydromorphone Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydromorphone Hydrochloride NDC 72865-171
- Generic Name
- Hydromorphone Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Your Military Exchanges
NDC Product
Human Otc DrugEthyl Rubbing Alcohol NDC 55301-876
- Generic Name
- Ethyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Zydus Lifesciences Limited
NDC Product
Human Prescription DrugOmeprazole NDC 65841-759
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOmeprazole NDC 65841-760
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOmeprazole NDC 65841-761
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Zydus Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugOmeprazole NDC 68382-411
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOmeprazole NDC 68382-412
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOmeprazole NDC 68382-500
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
