Home > National Drug Code (NDC) > MINERAL OIL, PRAMOXINE HYDROCHLORIDE AND ZINC OXIDE

MINERAL OIL, PRAMOXINE HYDROCHLORIDE AND ZINC OXIDE - 59779-399-03 - (MINERAL OIL, PRAMOXINE HYDROCHLORIDE AND ZINC OXIDE)

Alphabetical Index


Drug Information of MINERAL OIL, PRAMOXINE HYDROCHLORIDE AND ZINC OXIDE

Product NDC: 59779-399
Proprietary Name: MINERAL OIL, PRAMOXINE HYDROCHLORIDE AND ZINC OXIDE
Non Proprietary Name: MINERAL OIL, PRAMOXINE HYDROCHLORIDE AND ZINC OXIDE
Active Ingredient(s): 466; 10; 125    mg/g; mg/g; mg/g & nbsp;   MINERAL OIL, PRAMOXINE HYDROCHLORIDE AND ZINC OXIDE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of MINERAL OIL, PRAMOXINE HYDROCHLORIDE AND ZINC OXIDE

Product NDC: 59779-399
Labeler Name: CVS Pharmacy
Product Type: HUMAN OTC DRUG
FDA Application Number: part346
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100716

Package Information of MINERAL OIL, PRAMOXINE HYDROCHLORIDE AND ZINC OXIDE

Package NDC: 59779-399-03
Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON (59779-399-03) > 28 g in 1 TUBE, WITH APPLICATOR

NDC Information of MINERAL OIL, PRAMOXINE HYDROCHLORIDE AND ZINC OXIDE

NDC Code 59779-399-03
Proprietary Name MINERAL OIL, PRAMOXINE HYDROCHLORIDE AND ZINC OXIDE
Package Description 1 TUBE, WITH APPLICATOR in 1 CARTON (59779-399-03) > 28 g in 1 TUBE, WITH APPLICATOR
Product NDC 59779-399
Product Type Name HUMAN OTC DRUG
Non Proprietary Name MINERAL OIL, PRAMOXINE HYDROCHLORIDE AND ZINC OXIDE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20100716
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name CVS Pharmacy
Substance Name MINERAL OIL; PRAMOXINE HYDROCHLORIDE; ZINC OXIDE
Strength Number 466; 10; 125
Strength Unit mg/g; mg/g; mg/g
Pharmaceutical Classes

Complete Information of MINERAL OIL, PRAMOXINE HYDROCHLORIDE AND ZINC OXIDE


General Information