| 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 |