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Eczemin
Eczemin - 52389-628-04 - (Pramoxine Hydrochloride)
Drug Information of Eczemin
| Product NDC: | 52389-628 |
| Proprietary Name: | Eczemin |
| Non Proprietary Name: | Pramoxine Hydrochloride |
| Active Ingredient(s): | 10 mg/g & nbsp; Pramoxine Hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Eczemin
| Product NDC: | 52389-628 |
| Labeler Name: | Alva-Amco Pharmacal Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111116 |
Package Information of Eczemin
| Package NDC: | 52389-628-04 |
| Package Description: | 1 JAR in 1 CARTON (52389-628-04) > 113 g in 1 JAR |
NDC Information of Eczemin
| NDC Code | 52389-628-04 |
| Proprietary Name | Eczemin |
| Package Description | 1 JAR in 1 CARTON (52389-628-04) > 113 g in 1 JAR |
| Product NDC | 52389-628 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pramoxine Hydrochloride |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20111116 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Alva-Amco Pharmacal Companies, Inc. |
| Substance Name | PRAMOXINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
