Product NDC: | 67510-0054 |
Proprietary Name: | Anti Itch |
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: | 67510-0054 |
Labeler Name: | Kareway Product, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part336 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110811 |
Package NDC: | 67510-0054-2 |
Package Description: | 1 TUBE in 1 BOX (67510-0054-2) > 57 g in 1 TUBE |
NDC Code | 67510-0054-2 |
Proprietary Name | Anti Itch |
Package Description | 1 TUBE in 1 BOX (67510-0054-2) > 57 g in 1 TUBE |
Product NDC | 67510-0054 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Diphenhydramine HCl, Zinc acetate |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20110811 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Kareway Product, Inc. |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE |
Strength Number | 2; .1 |
Strength Unit | g/100g; g/100g |
Pharmaceutical Classes |