| Product NDC: | 51531-0332 |
| Proprietary Name: | MKMen Moisturizer Sunscreen Broad Spectrum SPF 25 |
| Non Proprietary Name: | avobenzone, homosalate, octinoxate, octisalate, oxybenzone |
| Active Ingredient(s): | 3; 10; 7.5; 5; 5 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL & nbsp; avobenzone, homosalate, octinoxate, octisalate, oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51531-0332 |
| Labeler Name: | Mary Kay Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20070616 |
| Package NDC: | 51531-0332-3 |
| Package Description: | 1 TUBE in 1 CARTON (51531-0332-3) > 88 mL in 1 TUBE |
| NDC Code | 51531-0332-3 |
| Proprietary Name | MKMen Moisturizer Sunscreen Broad Spectrum SPF 25 |
| Package Description | 1 TUBE in 1 CARTON (51531-0332-3) > 88 mL in 1 TUBE |
| Product NDC | 51531-0332 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | avobenzone, homosalate, octinoxate, octisalate, oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20070616 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Mary Kay Inc. |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 3; 10; 7.5; 5; 5 |
| Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes |