Product NDC: | 24286-1560 |
Proprietary Name: | Maximum Strength Hydrocortisone |
Non Proprietary Name: | HYDROCORTISONE |
Active Ingredient(s): | 1 g/100g & nbsp; HYDROCORTISONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 24286-1560 |
Labeler Name: | DLC Laboratories, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130322 |
Package NDC: | 24286-1560-1 |
Package Description: | 1 TUBE in 1 BOX (24286-1560-1) > 28 g in 1 TUBE |
NDC Code | 24286-1560-1 |
Proprietary Name | Maximum Strength Hydrocortisone |
Package Description | 1 TUBE in 1 BOX (24286-1560-1) > 28 g in 1 TUBE |
Product NDC | 24286-1560 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | HYDROCORTISONE |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20130322 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | DLC Laboratories, Inc |
Substance Name | HYDROCORTISONE |
Strength Number | 1 |
Strength Unit | g/100g |
Pharmaceutical Classes |