Product NDC: | 63824-309 |
Proprietary Name: | Clearasil |
Non Proprietary Name: | Benzoyl Peroxide |
Active Ingredient(s): | 10 g/100g & nbsp; Benzoyl Peroxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63824-309 |
Labeler Name: | Reckitt Benckiser LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333D |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110730 |
Package NDC: | 63824-309-01 |
Package Description: | 1 TUBE in 1 CARTON (63824-309-01) > 28 g in 1 TUBE |
NDC Code | 63824-309-01 |
Proprietary Name | Clearasil |
Package Description | 1 TUBE in 1 CARTON (63824-309-01) > 28 g in 1 TUBE |
Product NDC | 63824-309 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzoyl Peroxide |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20110730 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Reckitt Benckiser LLC |
Substance Name | BENZOYL PEROXIDE |
Strength Number | 10 |
Strength Unit | g/100g |
Pharmaceutical Classes |