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Benzoyl Peroxide
Benzoyl Peroxide - 67405-835-12 - (Benzoyl Peroxide)
Drug Information of Benzoyl Peroxide
| Product NDC: | 67405-835 |
| Proprietary Name: | Benzoyl Peroxide |
| Non Proprietary Name: | Benzoyl Peroxide |
| Active Ingredient(s): | 60 mg/mL & nbsp; Benzoyl Peroxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Benzoyl Peroxide
| Product NDC: | 67405-835 |
| Labeler Name: | Harris Pharmaceutical, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111118 |
Package Information of Benzoyl Peroxide
| Package NDC: | 67405-835-12 |
| Package Description: | 355 mL in 1 BOTTLE (67405-835-12) |
NDC Information of Benzoyl Peroxide
| NDC Code | 67405-835-12 |
| Proprietary Name | Benzoyl Peroxide |
| Package Description | 355 mL in 1 BOTTLE (67405-835-12) |
| Product NDC | 67405-835 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzoyl Peroxide |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20111118 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Harris Pharmaceutical, Inc. |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 60 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
