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MaxClarity
MaxClarity - 0145-2832-09 - (benzoyl peroxide)
Drug Information of MaxClarity
| Product NDC: | 0145-2832 |
| Proprietary Name: | MaxClarity |
| Non Proprietary Name: | benzoyl peroxide |
| Active Ingredient(s): | 25 mg/g & nbsp; benzoyl peroxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MaxClarity
| Product NDC: | 0145-2832 |
| Labeler Name: | Stiefel Laboratories Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110622 |
Package Information of MaxClarity
| Package NDC: | 0145-2832-09 |
| Package Description: | 1 TUBE in 1 CARTON (0145-2832-09) > 156 g in 1 TUBE |
NDC Information of MaxClarity
| NDC Code | 0145-2832-09 |
| Proprietary Name | MaxClarity |
| Package Description | 1 TUBE in 1 CARTON (0145-2832-09) > 156 g in 1 TUBE |
| Product NDC | 0145-2832 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | benzoyl peroxide |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110622 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Stiefel Laboratories Inc |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 25 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
