Product NDC: | 51143-066 |
Proprietary Name: | Live Better |
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) |
Product NDC: | 51143-066 |
Labeler Name: | The Great Atlantic & Pacific Tea Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20050920 |
Package NDC: | 51143-066-02 |
Package Description: | 1 TUBE in 1 CARTON (51143-066-02) > 28.4 g in 1 TUBE |
NDC Code | 51143-066-02 |
Proprietary Name | Live Better |
Package Description | 1 TUBE in 1 CARTON (51143-066-02) > 28.4 g in 1 TUBE |
Product NDC | 51143-066 |
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 | The Great Atlantic & Pacific Tea Company |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE |
Strength Number | 20; 1 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes |