Anti-Itch - 49348-992-30 - (Diphenhydramine HCL, Zinc Acetate)

Alphabetical Index


Drug Information of Anti-Itch

Product NDC: 49348-992
Proprietary Name: Anti-Itch
Non Proprietary Name: Diphenhydramine HCL, Zinc Acetate
Active Ingredient(s): 18; .882    mg/mL; mg/mL & nbsp;   Diphenhydramine HCL, Zinc Acetate
Administration Route(s): TOPICAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of Anti-Itch

Product NDC: 49348-992
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110615

Package Information of Anti-Itch

Package NDC: 49348-992-30
Package Description: 59 mL in 1 BOTTLE, SPRAY (49348-992-30)

NDC Information of Anti-Itch

NDC Code 49348-992-30
Proprietary Name Anti-Itch
Package Description 59 mL in 1 BOTTLE, SPRAY (49348-992-30)
Product NDC 49348-992
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Diphenhydramine HCL, Zinc Acetate
Dosage Form Name SPRAY
Route Name TOPICAL
Start Marketing Date 20110615
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name McKesson
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE
Strength Number 18; .882
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Anti-Itch


General Information