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Diphenhydramine Hydrochloride and Zinc Acetate
Diphenhydramine Hydrochloride and Zinc Acetate - 51672-2089-2 - (Diphenhydramine Hydrochloride and Zinc Acetate)
Drug Information of Diphenhydramine Hydrochloride and Zinc Acetate
| Product NDC: | 51672-2089 |
| Proprietary Name: | Diphenhydramine Hydrochloride and Zinc Acetate |
| Non Proprietary Name: | Diphenhydramine Hydrochloride and Zinc Acetate |
| Active Ingredient(s): | 2; .1 g/100g; g/100g & nbsp; Diphenhydramine Hydrochloride and Zinc Acetate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diphenhydramine Hydrochloride and Zinc Acetate
| Product NDC: | 51672-2089 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20080801 |
Package Information of Diphenhydramine Hydrochloride and Zinc Acetate
| Package NDC: | 51672-2089-2 |
| Package Description: | 1 TUBE in 1 CARTON (51672-2089-2) > 28.4 g in 1 TUBE |
NDC Information of Diphenhydramine Hydrochloride and Zinc Acetate
| NDC Code | 51672-2089-2 |
| Proprietary Name | Diphenhydramine Hydrochloride and Zinc Acetate |
| Package Description | 1 TUBE in 1 CARTON (51672-2089-2) > 28.4 g in 1 TUBE |
| Product NDC | 51672-2089 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine Hydrochloride and Zinc Acetate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20080801 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE |
| Strength Number | 2; .1 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |
