Product NDC: | 58232-4010 |
Proprietary Name: | Neosporin Eczema Essentials |
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) |
Product NDC: | 58232-4010 |
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: | 20110930 |
Package NDC: | 58232-4010-1 |
Package Description: | 1 TUBE in 1 CARTON (58232-4010-1) > 28 g in 1 TUBE |
NDC Code | 58232-4010-1 |
Proprietary Name | Neosporin Eczema Essentials |
Package Description | 1 TUBE in 1 CARTON (58232-4010-1) > 28 g in 1 TUBE |
Product NDC | 58232-4010 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Hydrocortisone |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20110930 |
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 |