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DDF Benzoyl Peroxide
DDF Benzoyl Peroxide - 37000-708-56 - (Benzoyl Peroxide)
Drug Information of DDF Benzoyl Peroxide
| Product NDC: | 37000-708 |
| Proprietary Name: | DDF Benzoyl Peroxide |
| Non Proprietary Name: | Benzoyl Peroxide |
| Active Ingredient(s): | 50 mg/g & nbsp; Benzoyl Peroxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DDF Benzoyl Peroxide
| Product NDC: | 37000-708 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20080501 |
Package Information of DDF Benzoyl Peroxide
| Package NDC: | 37000-708-56 |
| Package Description: | 1 TUBE in 1 CARTON (37000-708-56) > 56 g in 1 TUBE |
NDC Information of DDF Benzoyl Peroxide
| NDC Code | 37000-708-56 |
| Proprietary Name | DDF Benzoyl Peroxide |
| Package Description | 1 TUBE in 1 CARTON (37000-708-56) > 56 g in 1 TUBE |
| Product NDC | 37000-708 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzoyl Peroxide |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20080501 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 50 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
