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Oxy Face Wash
Oxy Face Wash - 10742-8219-1 - (Benzoyl Peroxide)
Drug Information of Oxy Face Wash
| Product NDC: | 10742-8219 |
| Proprietary Name: | Oxy Face Wash |
| Non Proprietary Name: | Benzoyl Peroxide |
| Active Ingredient(s): | 50 mg/mL & nbsp; Benzoyl Peroxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxy Face Wash
| Product NDC: | 10742-8219 |
| Labeler Name: | The Mentholatum Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120201 |
Package Information of Oxy Face Wash
| Package NDC: | 10742-8219-1 |
| Package Description: | 177 mL in 1 BOTTLE (10742-8219-1) |
NDC Information of Oxy Face Wash
| NDC Code | 10742-8219-1 |
| Proprietary Name | Oxy Face Wash |
| Package Description | 177 mL in 1 BOTTLE (10742-8219-1) |
| Product NDC | 10742-8219 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzoyl Peroxide |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | The Mentholatum Company |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
