| 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 |