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CVS Extra Strength Itch Relief
CVS Extra Strength Itch Relief - 59779-053-03 - (DIPHENHYDRAMINE HYDROCHLORIDE and ZINC ACETATE)
Drug Information of CVS Extra Strength Itch Relief
| Product NDC: | 59779-053 |
| Proprietary Name: | CVS Extra Strength Itch Relief |
| Non Proprietary Name: | DIPHENHYDRAMINE HYDROCHLORIDE and ZINC ACETATE |
| Active Ingredient(s): | 20; 12 mg/g; mg/g & nbsp; DIPHENHYDRAMINE HYDROCHLORIDE and ZINC ACETATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CVS Extra Strength Itch Relief
| Product NDC: | 59779-053 |
| Labeler Name: | CVS Pharmacy |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100913 |
Package Information of CVS Extra Strength Itch Relief
| Package NDC: | 59779-053-03 |
| Package Description: | 1 TUBE in 1 CARTON (59779-053-03) > 28 g in 1 TUBE |
NDC Information of CVS Extra Strength Itch Relief
| NDC Code | 59779-053-03 |
| Proprietary Name | CVS Extra Strength Itch Relief |
| Package Description | 1 TUBE in 1 CARTON (59779-053-03) > 28 g in 1 TUBE |
| Product NDC | 59779-053 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DIPHENHYDRAMINE HYDROCHLORIDE and ZINC ACETATE |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20100913 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CVS Pharmacy |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE |
| Strength Number | 20; 12 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
