Home
>
National Drug Code (NDC)
>
Aveeno Hydrocortisone Anti Itch
Aveeno Hydrocortisone Anti Itch - 58232-1402-1 - (Hydrocortisone)
Drug Information of Aveeno Hydrocortisone Anti Itch
| Product NDC: | 58232-1402 |
| Proprietary Name: | Aveeno Hydrocortisone Anti Itch |
| Non Proprietary Name: | Hydrocortisone |
| Active Ingredient(s): | 10 mg/g & nbsp; Hydrocortisone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aveeno Hydrocortisone Anti Itch
| Product NDC: | 58232-1402 |
| 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: | 20121008 |
Package Information of Aveeno Hydrocortisone Anti Itch
| Package NDC: | 58232-1402-1 |
| Package Description: | 1 TUBE in 1 CARTON (58232-1402-1) > 28 g in 1 TUBE |
NDC Information of Aveeno Hydrocortisone Anti Itch
| NDC Code | 58232-1402-1 |
| Proprietary Name | Aveeno Hydrocortisone Anti Itch |
| Package Description | 1 TUBE in 1 CARTON (58232-1402-1) > 28 g in 1 TUBE |
| Product NDC | 58232-1402 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hydrocortisone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20121008 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | HYDROCORTISONE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
