Product NDC: | 49314-5801 |
Proprietary Name: | Hydrocortisone |
Non Proprietary Name: | Hydrocortisone |
Active Ingredient(s): | 10 mg/mL & nbsp; Hydrocortisone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49314-5801 |
Labeler Name: | UniShield |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100728 |
Package NDC: | 49314-5801-0 |
Package Description: | .8 mL in 1 PACKET (49314-5801-0) |
NDC Code | 49314-5801-0 |
Proprietary Name | Hydrocortisone |
Package Description | .8 mL in 1 PACKET (49314-5801-0) |
Product NDC | 49314-5801 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Hydrocortisone |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20100728 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | UniShield |
Substance Name | HYDROCORTISONE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes |