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Cortaid
Cortaid - 58232-0406-2 - (Hydrocortisone Acetate)
Drug Information of Cortaid
| Product NDC: | 58232-0406 |
| Proprietary Name: | Cortaid |
| Non Proprietary Name: | Hydrocortisone Acetate |
| Active Ingredient(s): | 1 g/100g & nbsp; Hydrocortisone Acetate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cortaid
| Product NDC: | 58232-0406 |
| 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: | 20091030 |
Package Information of Cortaid
| Package NDC: | 58232-0406-2 |
| Package Description: | 1 TUBE in 1 CARTON (58232-0406-2) > 37.7 g in 1 TUBE |
NDC Information of Cortaid
| NDC Code | 58232-0406-2 |
| Proprietary Name | Cortaid |
| Package Description | 1 TUBE in 1 CARTON (58232-0406-2) > 37.7 g in 1 TUBE |
| Product NDC | 58232-0406 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hydrocortisone Acetate |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20091030 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson consumer Companies, Inc. |
| Substance Name | HYDROCORTISONE ACETATE |
| Strength Number | 1 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
