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Aveeno Anti Itch Concentrated
Aveeno Anti Itch Concentrated - 58232-9910-2 - (Zinc Oxide, Ferric Oxide Red, and Pramoxine Hydrochloride)
Drug Information of Aveeno Anti Itch Concentrated
| Product NDC: | 58232-9910 |
| Proprietary Name: | Aveeno Anti Itch Concentrated |
| Non Proprietary Name: | Zinc Oxide, Ferric Oxide Red, and Pramoxine Hydrochloride |
| Active Ingredient(s): | .6; 10; 29.4 mg/mL; mg/mL; mg/mL & nbsp; Zinc Oxide, Ferric Oxide Red, and Pramoxine Hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aveeno Anti Itch Concentrated
| Product NDC: | 58232-9910 |
| 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: | 20121107 |
Package Information of Aveeno Anti Itch Concentrated
| Package NDC: | 58232-9910-2 |
| Package Description: | 118 mL in 1 BOTTLE (58232-9910-2) |
NDC Information of Aveeno Anti Itch Concentrated
| NDC Code | 58232-9910-2 |
| Proprietary Name | Aveeno Anti Itch Concentrated |
| Package Description | 118 mL in 1 BOTTLE (58232-9910-2) |
| Product NDC | 58232-9910 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide, Ferric Oxide Red, and Pramoxine Hydrochloride |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20121107 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | FERRIC OXIDE RED; PRAMOXINE HYDROCHLORIDE; ZINC OXIDE |
| Strength Number | .6; 10; 29.4 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
