Product NDC: | 51531-7497 |
Proprietary Name: | Mary Kay Tinted Moisturizer Sunscreen SPF 20 Bronze 1 |
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: | 51531-7497 |
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: | 51531-7497-8 |
Package Description: | 1 TUBE in 1 CARTON (51531-7497-8) > 43 mL in 1 TUBE |
NDC Code | 51531-7497-8 |
Proprietary Name | Mary Kay Tinted Moisturizer Sunscreen SPF 20 Bronze 1 |
Package Description | 1 TUBE in 1 CARTON (51531-7497-8) > 43 mL in 1 TUBE |
Product NDC | 51531-7497 |
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 |