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Dermarest
Dermarest - 63736-325-24 - (Pramoxine Hydrochloride)
Drug Information of Dermarest
| Product NDC: | 63736-325 |
| Proprietary Name: | Dermarest |
| Non Proprietary Name: | Pramoxine Hydrochloride |
| Active Ingredient(s): | 1 g/57g & nbsp; Pramoxine Hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dermarest
| Product NDC: | 63736-325 |
| Labeler Name: | Insight Pharmaceuticals LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100723 |
Package Information of Dermarest
| Package NDC: | 63736-325-24 |
| Package Description: | 1 TUBE in 1 CARTON (63736-325-24) > 56.7 g in 1 TUBE |
NDC Information of Dermarest
| NDC Code | 63736-325-24 |
| Proprietary Name | Dermarest |
| Package Description | 1 TUBE in 1 CARTON (63736-325-24) > 56.7 g in 1 TUBE |
| Product NDC | 63736-325 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pramoxine Hydrochloride |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100723 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Insight Pharmaceuticals LLC |
| Substance Name | PRAMOXINE HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | g/57g |
| Pharmaceutical Classes |
