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Mary Kay Acne Treatment
Mary Kay Acne Treatment - 51531-0813-1 - (Benzoyl Peroxide)
Drug Information of Mary Kay Acne Treatment
| Product NDC: | 51531-0813 |
| Proprietary Name: | Mary Kay Acne Treatment |
| Non Proprietary Name: | Benzoyl Peroxide |
| Active Ingredient(s): | 5 g/100g & nbsp; Benzoyl Peroxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mary Kay Acne Treatment
| Product NDC: | 51531-0813 |
| Labeler Name: | Mary Kay Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19880119 |
Package Information of Mary Kay Acne Treatment
| Package NDC: | 51531-0813-1 |
| Package Description: | 1 TUBE in 1 CARTON (51531-0813-1) > 28 g in 1 TUBE |
NDC Information of Mary Kay Acne Treatment
| NDC Code | 51531-0813-1 |
| Proprietary Name | Mary Kay Acne Treatment |
| Package Description | 1 TUBE in 1 CARTON (51531-0813-1) > 28 g in 1 TUBE |
| Product NDC | 51531-0813 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzoyl Peroxide |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 19880119 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Mary Kay Inc. |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 5 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
