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 |