Product NDC: | 59779-399 |
Proprietary Name: | MINERAL OIL, PRAMOXINE HYDROCHLORIDE AND ZINC OXIDE |
Non Proprietary Name: | MINERAL OIL, PRAMOXINE HYDROCHLORIDE AND ZINC OXIDE |
Active Ingredient(s): | 466; 10; 125 mg/g; mg/g; mg/g & nbsp; MINERAL OIL, PRAMOXINE HYDROCHLORIDE AND ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-399 |
Labeler Name: | CVS Pharmacy |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part346 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100716 |
Package NDC: | 59779-399-03 |
Package Description: | 1 TUBE, WITH APPLICATOR in 1 CARTON (59779-399-03) > 28 g in 1 TUBE, WITH APPLICATOR |
NDC Code | 59779-399-03 |
Proprietary Name | MINERAL OIL, PRAMOXINE HYDROCHLORIDE AND ZINC OXIDE |
Package Description | 1 TUBE, WITH APPLICATOR in 1 CARTON (59779-399-03) > 28 g in 1 TUBE, WITH APPLICATOR |
Product NDC | 59779-399 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | MINERAL OIL, PRAMOXINE HYDROCHLORIDE AND ZINC OXIDE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20100716 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | CVS Pharmacy |
Substance Name | MINERAL OIL; PRAMOXINE HYDROCHLORIDE; ZINC OXIDE |
Strength Number | 466; 10; 125 |
Strength Unit | mg/g; mg/g; mg/g |
Pharmaceutical Classes |