Ivarest - 10157-9077-1 - (Zinc Oxide, Benzyl Alcohol, and Diphenhydramine Hydrochloride)

Alphabetical Index


Drug Information of Ivarest

Product NDC: 10157-9077
Proprietary Name: Ivarest
Non Proprietary Name: Zinc Oxide, Benzyl Alcohol, and Diphenhydramine Hydrochloride
Active Ingredient(s): 10.5; 2; 14    g/100g; g/100g; g/100g & nbsp;   Zinc Oxide, Benzyl Alcohol, and Diphenhydramine Hydrochloride
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Ivarest

Product NDC: 10157-9077
Labeler Name: Blistex Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part347
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20071231

Package Information of Ivarest

Package NDC: 10157-9077-1
Package Description: 1 TUBE in 1 CARTON (10157-9077-1) > 56 g in 1 TUBE

NDC Information of Ivarest

NDC Code 10157-9077-1
Proprietary Name Ivarest
Package Description 1 TUBE in 1 CARTON (10157-9077-1) > 56 g in 1 TUBE
Product NDC 10157-9077
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Zinc Oxide, Benzyl Alcohol, and Diphenhydramine Hydrochloride
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20071231
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Blistex Inc
Substance Name BENZYL ALCOHOL; DIPHENHYDRAMINE HYDROCHLORIDE; ZINC OXIDE
Strength Number 10.5; 2; 14
Strength Unit g/100g; g/100g; g/100g
Pharmaceutical Classes

Complete Information of Ivarest


General Information