Product NDC: | 42853-102 |
Proprietary Name: | ALL-IN-ONE |
Non Proprietary Name: | BENZOYL PEROXIDE |
Active Ingredient(s): | 5.5 g/100mL & nbsp; BENZOYL PEROXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42853-102 |
Labeler Name: | AUGUSTUS BIOMED LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333D |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120225 |
Package NDC: | 42853-102-13 |
Package Description: | 100 mL in 1 TUBE (42853-102-13) |
NDC Code | 42853-102-13 |
Proprietary Name | ALL-IN-ONE |
Package Description | 100 mL in 1 TUBE (42853-102-13) |
Product NDC | 42853-102 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BENZOYL PEROXIDE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120225 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | AUGUSTUS BIOMED LLC |
Substance Name | BENZOYL PEROXIDE |
Strength Number | 5.5 |
Strength Unit | g/100mL |
Pharmaceutical Classes |