Product NDC: | 0536-4089 |
Proprietary Name: | Acne Medication 5 |
Non Proprietary Name: | Benzoyl Peroxide |
Active Ingredient(s): | 50 mg/g & nbsp; Benzoyl Peroxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0536-4089 |
Labeler Name: | Rugby Laboratories |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333D |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20121029 |
Package NDC: | 0536-4089-56 |
Package Description: | 1 TUBE in 1 CARTON (0536-4089-56) > 42.5 g in 1 TUBE |
NDC Code | 0536-4089-56 |
Proprietary Name | Acne Medication 5 |
Package Description | 1 TUBE in 1 CARTON (0536-4089-56) > 42.5 g in 1 TUBE |
Product NDC | 0536-4089 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzoyl Peroxide |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20121029 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Rugby Laboratories |
Substance Name | BENZOYL PEROXIDE |
Strength Number | 50 |
Strength Unit | mg/g |
Pharmaceutical Classes |