Product NDC: | 51531-0850 |
Proprietary Name: | Mary Kay Foundation Primer |
Non Proprietary Name: | avobenzone, homosalate, octisalate, octocrylene |
Active Ingredient(s): | 2.5; 9; 5; 3 g/100mL; g/100mL; g/100mL; g/100mL & nbsp; avobenzone, homosalate, octisalate, octocrylene |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51531-0850 |
Labeler Name: | Mary Kay Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120301 |
Package NDC: | 51531-0850-1 |
Package Description: | 1 TUBE in 1 CARTON (51531-0850-1) > 29 mL in 1 TUBE |
NDC Code | 51531-0850-1 |
Proprietary Name | Mary Kay Foundation Primer |
Package Description | 1 TUBE in 1 CARTON (51531-0850-1) > 29 mL in 1 TUBE |
Product NDC | 51531-0850 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | avobenzone, homosalate, octisalate, octocrylene |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20120301 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Mary Kay Inc. |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE |
Strength Number | 2.5; 9; 5; 3 |
Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL |
Pharmaceutical Classes |