Product NDC: | 0179-8704 |
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): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0179-8704 |
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: | 0179-8704-05 |
Package Description: | 142 g in 1 BOTTLE (0179-8704-05) |
NDC Code | 0179-8704-05 |
Proprietary Name | kaiser permanente benzoyl peroxide |
Package Description | 142 g in 1 BOTTLE (0179-8704-05) |
Product NDC | 0179-8704 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BENZOYL PEROXIDE |
Dosage Form Name | LIQUID |
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 |