| Product NDC: | 0179-8703 |
| Proprietary Name: | kaiser permanente benzoyl peroxide |
| Non Proprietary Name: | BENZOYL PEROXIDE |
| Active Ingredient(s): | 10 g/100g & nbsp; BENZOYL PEROXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0179-8703 |
| Labeler Name: | Kaiser Foundation Hospitals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20070608 |
| Package NDC: | 0179-8703-60 |
| Package Description: | 1 TUBE in 1 CARTON (0179-8703-60) > 56.7 g in 1 TUBE |
| NDC Code | 0179-8703-60 |
| Proprietary Name | kaiser permanente benzoyl peroxide |
| Package Description | 1 TUBE in 1 CARTON (0179-8703-60) > 56.7 g in 1 TUBE |
| Product NDC | 0179-8703 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZOYL PEROXIDE |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20070608 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Kaiser Foundation Hospitals |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 10 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |