sunmark - 49348-854-72 - (diphenhydramine hydrochloride and zinc acetate)

Alphabetical Index


Drug Information of sunmark

Product NDC: 49348-854
Proprietary Name: sunmark
Non Proprietary Name: diphenhydramine hydrochloride and zinc acetate
Active Ingredient(s): 20; 1    mg/g; mg/g & nbsp;   diphenhydramine hydrochloride and zinc acetate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of sunmark

Product NDC: 49348-854
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20050920

Package Information of sunmark

Package NDC: 49348-854-72
Package Description: 1 TUBE in 1 CARTON (49348-854-72) > 28.4 g in 1 TUBE

NDC Information of sunmark

NDC Code 49348-854-72
Proprietary Name sunmark
Package Description 1 TUBE in 1 CARTON (49348-854-72) > 28.4 g in 1 TUBE
Product NDC 49348-854
Product Type Name HUMAN OTC DRUG
Non Proprietary Name diphenhydramine hydrochloride and zinc acetate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20050920
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McKesson
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE
Strength Number 20; 1
Strength Unit mg/g; mg/g
Pharmaceutical Classes

Complete Information of sunmark


General Information