Product NDC: | 49348-992 |
Proprietary Name: | Anti-Itch |
Non Proprietary Name: | Diphenhydramine HCL, Zinc Acetate |
Active Ingredient(s): | 18; .882 mg/mL; mg/mL & nbsp; Diphenhydramine HCL, Zinc Acetate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49348-992 |
Labeler Name: | McKesson |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110615 |
Package NDC: | 49348-992-30 |
Package Description: | 59 mL in 1 BOTTLE, SPRAY (49348-992-30) |
NDC Code | 49348-992-30 |
Proprietary Name | Anti-Itch |
Package Description | 59 mL in 1 BOTTLE, SPRAY (49348-992-30) |
Product NDC | 49348-992 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Diphenhydramine HCL, Zinc Acetate |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20110615 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | McKesson |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE |
Strength Number | 18; .882 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |