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CVS Medicated Anti-Itch
CVS Medicated Anti-Itch - 59779-621-64 - (MENTHOL, PRAMOXINE HYDROCHLORIDE)
Drug Information of CVS Medicated Anti-Itch
| Product NDC: | 59779-621 |
| Proprietary Name: | CVS Medicated Anti-Itch |
| Non Proprietary Name: | MENTHOL, PRAMOXINE HYDROCHLORIDE |
| Active Ingredient(s): | 10; 10 mg/g; mg/g & nbsp; MENTHOL, PRAMOXINE HYDROCHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CVS Medicated Anti-Itch
| Product NDC: | 59779-621 |
| Labeler Name: | CVS Pharmacy |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100708 |
Package Information of CVS Medicated Anti-Itch
| Package NDC: | 59779-621-64 |
| Package Description: | 1 TUBE in 1 CARTON (59779-621-64) > 56 g in 1 TUBE |
NDC Information of CVS Medicated Anti-Itch
| NDC Code | 59779-621-64 |
| Proprietary Name | CVS Medicated Anti-Itch |
| Package Description | 1 TUBE in 1 CARTON (59779-621-64) > 56 g in 1 TUBE |
| Product NDC | 59779-621 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MENTHOL, PRAMOXINE HYDROCHLORIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100708 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | CVS Pharmacy |
| Substance Name | MENTHOL; PRAMOXINE HYDROCHLORIDE |
| Strength Number | 10; 10 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
