| Product NDC: | 51531-7502 |
| Proprietary Name: | Mary Kay Tinted Moisturizer Sunscreen SPF 20 Bronze 2 |
| Non Proprietary Name: | octinoxate, octisalate, zinc oxide, oxybenzone, |
| Active Ingredient(s): | 7.5; 5; 1.75; 2.4 g/100mL; g/100mL; g/100mL; g/100mL & nbsp; octinoxate, octisalate, zinc oxide, oxybenzone, |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51531-7502 |
| Labeler Name: | Mary Kay Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20060816 |
| Package NDC: | 51531-7502-8 |
| Package Description: | 1 TUBE in 1 CARTON (51531-7502-8) > 43 mL in 1 TUBE |
| NDC Code | 51531-7502-8 |
| Proprietary Name | Mary Kay Tinted Moisturizer Sunscreen SPF 20 Bronze 2 |
| Package Description | 1 TUBE in 1 CARTON (51531-7502-8) > 43 mL in 1 TUBE |
| Product NDC | 51531-7502 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | octinoxate, octisalate, zinc oxide, oxybenzone, |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20060816 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Mary Kay Inc. |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE; ZINC OXIDE |
| Strength Number | 7.5; 5; 1.75; 2.4 |
| Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes |