| Product NDC: | 64760-209 |
| Proprietary Name: | acne treatment |
| Non Proprietary Name: | benzoyl peroxide |
| Active Ingredient(s): | 5.6 g/56g & nbsp; benzoyl peroxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 64760-209 |
| Labeler Name: | Glytone |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100301 |
| Package NDC: | 64760-209-01 |
| Package Description: | 1 TUBE in 1 BOX (64760-209-01) > 56 g in 1 TUBE |
| NDC Code | 64760-209-01 |
| Proprietary Name | acne treatment |
| Package Description | 1 TUBE in 1 BOX (64760-209-01) > 56 g in 1 TUBE |
| Product NDC | 64760-209 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | benzoyl peroxide |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100301 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Glytone |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 5.6 |
| Strength Unit | g/56g |
| Pharmaceutical Classes |