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Aveeno Active Naturals Skin Relief Medicated Anti Itch Treatment
Aveeno Active Naturals Skin Relief Medicated Anti Itch Treatment - 58232-0036-1 - (Pramoxine Hydrochloride)
Drug Information of Aveeno Active Naturals Skin Relief Medicated Anti Itch Treatment
| Product NDC: | 58232-0036 |
| Proprietary Name: | Aveeno Active Naturals Skin Relief Medicated Anti Itch Treatment |
| Non Proprietary Name: | Pramoxine Hydrochloride |
| Active Ingredient(s): | 5 mg/g & nbsp; Pramoxine Hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aveeno Active Naturals Skin Relief Medicated Anti Itch Treatment
| Product NDC: | 58232-0036 |
| Labeler Name: | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110907 |
Package Information of Aveeno Active Naturals Skin Relief Medicated Anti Itch Treatment
| Package NDC: | 58232-0036-1 |
| Package Description: | 1 TUBE in 1 CARTON (58232-0036-1) > 156 g in 1 TUBE |
NDC Information of Aveeno Active Naturals Skin Relief Medicated Anti Itch Treatment
| NDC Code | 58232-0036-1 |
| Proprietary Name | Aveeno Active Naturals Skin Relief Medicated Anti Itch Treatment |
| Package Description | 1 TUBE in 1 CARTON (58232-0036-1) > 156 g in 1 TUBE |
| Product NDC | 58232-0036 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pramoxine Hydrochloride |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110907 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | PRAMOXINE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
