Product NDC: | 51141-0054 |
Proprietary Name: | Anti Itch Cream |
Non Proprietary Name: | Diphenhydramine HCl, Zinc acetate |
Active Ingredient(s): | 2; .1 g/100g; g/100g & nbsp; Diphenhydramine HCl, Zinc acetate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51141-0054 |
Labeler Name: | NeoPharm Co., Ltd. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part336 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100907 |
Package NDC: | 51141-0054-1 |
Package Description: | 1 TUBE in 1 BOX (51141-0054-1) > 28 g in 1 TUBE |
NDC Code | 51141-0054-1 |
Proprietary Name | Anti Itch Cream |
Package Description | 1 TUBE in 1 BOX (51141-0054-1) > 28 g in 1 TUBE |
Product NDC | 51141-0054 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Diphenhydramine HCl, Zinc acetate |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20100907 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | NeoPharm Co., Ltd. |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE |
Strength Number | 2; .1 |
Strength Unit | g/100g; g/100g |
Pharmaceutical Classes |