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BENZOYL PEROXIDE
BENZOYL PEROXIDE - 68752-034-08 - (BENZOYL PEROXIDE)
Drug Information of BENZOYL PEROXIDE
| Product NDC: | 68752-034 |
| Proprietary Name: | BENZOYL PEROXIDE |
| Non Proprietary Name: | BENZOYL PEROXIDE |
| Active Ingredient(s): | 50 mg/g & nbsp; BENZOYL PEROXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BENZOYL PEROXIDE
| Product NDC: | 68752-034 |
| Labeler Name: | TriMarc Labs |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20041116 |
Package Information of BENZOYL PEROXIDE
| Package NDC: | 68752-034-08 |
| Package Description: | 227 g in 1 BOTTLE, PLASTIC (68752-034-08) |
NDC Information of BENZOYL PEROXIDE
| NDC Code | 68752-034-08 |
| Proprietary Name | BENZOYL PEROXIDE |
| Package Description | 227 g in 1 BOTTLE, PLASTIC (68752-034-08) |
| Product NDC | 68752-034 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZOYL PEROXIDE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20041116 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | TriMarc Labs |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 50 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
