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Oxy Maximum Action Spot Treatment
Oxy Maximum Action Spot Treatment - 10742-8301-1 - (benzoyl peroxide)
Drug Information of Oxy Maximum Action Spot Treatment
| Product NDC: | 10742-8301 |
| Proprietary Name: | Oxy Maximum Action Spot Treatment |
| Non Proprietary Name: | benzoyl peroxide |
| Active Ingredient(s): | 100 mg/g & nbsp; benzoyl peroxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxy Maximum Action Spot Treatment
| Product NDC: | 10742-8301 |
| Labeler Name: | The Mentholatum Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130115 |
Package Information of Oxy Maximum Action Spot Treatment
| Package NDC: | 10742-8301-1 |
| Package Description: | 1 TUBE in 1 CARTON (10742-8301-1) > 18.4 g in 1 TUBE |
NDC Information of Oxy Maximum Action Spot Treatment
| NDC Code | 10742-8301-1 |
| Proprietary Name | Oxy Maximum Action Spot Treatment |
| Package Description | 1 TUBE in 1 CARTON (10742-8301-1) > 18.4 g in 1 TUBE |
| Product NDC | 10742-8301 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | benzoyl peroxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130115 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | The Mentholatum Company |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 100 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
