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Proactiv
Proactiv - 11410-401-09 - (Benzoyl Peroxide)
Drug Information of Proactiv
| Product NDC: | 11410-401 |
| Proprietary Name: | Proactiv |
| Non Proprietary Name: | Benzoyl Peroxide |
| Active Ingredient(s): | .06 g/g & nbsp; Benzoyl Peroxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Proactiv
| Product NDC: | 11410-401 |
| Labeler Name: | Guthy-Renker LLC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19990101 |
Package Information of Proactiv
| Package NDC: | 11410-401-09 |
| Package Description: | 1 TUBE in 1 CARTON (11410-401-09) > 9.45 g in 1 TUBE |
NDC Information of Proactiv
| NDC Code | 11410-401-09 |
| Proprietary Name | Proactiv |
| Package Description | 1 TUBE in 1 CARTON (11410-401-09) > 9.45 g in 1 TUBE |
| Product NDC | 11410-401 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzoyl Peroxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19990101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Guthy-Renker LLC. |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | .06 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
