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BenzEFoam Ultra
BenzEFoam Ultra - 16781-201-06 - (BENZOYL PEROXIDE)
Drug Information of BenzEFoam Ultra
| Product NDC: | 16781-201 |
| Proprietary Name: | BenzEFoam Ultra |
| Non Proprietary Name: | BENZOYL PEROXIDE |
| Active Ingredient(s): | 9.8 g/100g & nbsp; BENZOYL PEROXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BenzEFoam Ultra
| Product NDC: | 16781-201 |
| Labeler Name: | Onset Dermatologics LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110304 |
Package Information of BenzEFoam Ultra
| Package NDC: | 16781-201-06 |
| Package Description: | 6 CAN in 1 CARTON (16781-201-06) > 5 g in 1 CAN |
NDC Information of BenzEFoam Ultra
| NDC Code | 16781-201-06 |
| Proprietary Name | BenzEFoam Ultra |
| Package Description | 6 CAN in 1 CARTON (16781-201-06) > 5 g in 1 CAN |
| Product NDC | 16781-201 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | BENZOYL PEROXIDE |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110304 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Onset Dermatologics LLC |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 9.8 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
