Home > National Drug Code (NDC) > itch relief

itch relief - 37808-622-64 - (Diphenhydramine Hydrochloride, Zinc Acetate)

Alphabetical Index


Drug Information of itch relief

Product NDC: 37808-622
Proprietary Name: itch relief
Non Proprietary Name: Diphenhydramine Hydrochloride, Zinc Acetate
Active Ingredient(s): 2; .1    g/100g; g/100g & nbsp;   Diphenhydramine Hydrochloride, Zinc Acetate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of itch relief

Product NDC: 37808-622
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100915

Package Information of itch relief

Package NDC: 37808-622-64
Package Description: 1 TUBE in 1 CARTON (37808-622-64) > 28 g in 1 TUBE

NDC Information of itch relief

NDC Code 37808-622-64
Proprietary Name itch relief
Package Description 1 TUBE in 1 CARTON (37808-622-64) > 28 g in 1 TUBE
Product NDC 37808-622
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Diphenhydramine Hydrochloride, Zinc Acetate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20100915
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name H E B
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE
Strength Number 2; .1
Strength Unit g/100g; g/100g
Pharmaceutical Classes

Complete Information of itch relief


General Information