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OXY Clinical
OXY Clinical - 10742-8212-3 - (Benzoyl peroxide)
Drug Information of OXY Clinical
| Product NDC: | 10742-8212 |
| Proprietary Name: | OXY Clinical |
| Non Proprietary Name: | Benzoyl peroxide |
| Active Ingredient(s): | 50 mg/g & nbsp; Benzoyl peroxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OXY Clinical
| Product NDC: | 10742-8212 |
| Labeler Name: | The Mentholatum Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100601 |
Package Information of OXY Clinical
| Package NDC: | 10742-8212-3 |
| Package Description: | 19.8 g in 1 TUBE (10742-8212-3) |
NDC Information of OXY Clinical
| NDC Code | 10742-8212-3 |
| Proprietary Name | OXY Clinical |
| Package Description | 19.8 g in 1 TUBE (10742-8212-3) |
| Product NDC | 10742-8212 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzoyl peroxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100601 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | The Mentholatum Company |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 50 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
