Product NDC: | 41520-295 |
Proprietary Name: | Itch Relief |
Non Proprietary Name: | Diphenhydramine HCl, Zinc Acetate |
Active Ingredient(s): | 2; .1 kg/100L; kg/100L & nbsp; Diphenhydramine HCl, Zinc Acetate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41520-295 |
Labeler Name: | American Sales Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20111006 |
Package NDC: | 41520-295-16 |
Package Description: | .059 L in 1 BOTTLE, SPRAY (41520-295-16) |
NDC Code | 41520-295-16 |
Proprietary Name | Itch Relief |
Package Description | .059 L in 1 BOTTLE, SPRAY (41520-295-16) |
Product NDC | 41520-295 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Diphenhydramine HCl, Zinc Acetate |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20111006 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | American Sales Company |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE |
Strength Number | 2; .1 |
Strength Unit | kg/100L; kg/100L |
Pharmaceutical Classes |