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Benadryl Extra Strength - 58232-0741-1 - (Diphenhydramine Hydrochloride and Zinc Acetate)

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Drug Information of Benadryl Extra Strength

Product NDC: 58232-0741
Proprietary Name: Benadryl Extra Strength
Non Proprietary Name: Diphenhydramine Hydrochloride and Zinc Acetate
Active Ingredient(s): 2; 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 Benadryl Extra Strength

Product NDC: 58232-0741
Labeler Name: Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20121015

Package Information of Benadryl Extra Strength

Package NDC: 58232-0741-1
Package Description: 1 TUBE in 1 CARTON (58232-0741-1) > 28.3 g in 1 TUBE

NDC Information of Benadryl Extra Strength

NDC Code 58232-0741-1
Proprietary Name Benadryl Extra Strength
Package Description 1 TUBE in 1 CARTON (58232-0741-1) > 28.3 g in 1 TUBE
Product NDC 58232-0741
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Diphenhydramine Hydrochloride and Zinc Acetate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20121015
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE
Strength Number 2; 1
Strength Unit mg/g; mg/g
Pharmaceutical Classes

Complete Information of Benadryl Extra Strength


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