| 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 |