Product NDC: | 51531-8360 |
Proprietary Name: | Mary Kay TimeWise Day Solution SPF 35 |
Non Proprietary Name: | avobenzone, homosalate, octisalate, octocrylene, oxybenzone |
Active Ingredient(s): | 2; 10; 5; 2; 4 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL & nbsp; avobenzone, homosalate, octisalate, octocrylene, oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51531-8360 |
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: | 51531-8360-5 |
Package Description: | 14 mL in 1 BOTTLE, PUMP (51531-8360-5) |
NDC Code | 51531-8360-5 |
Proprietary Name | Mary Kay TimeWise Day Solution SPF 35 |
Package Description | 14 mL in 1 BOTTLE, PUMP (51531-8360-5) |
Product NDC | 51531-8360 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | avobenzone, homosalate, octisalate, octocrylene, oxybenzone |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20120301 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Mary Kay Inc. |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | 2; 10; 5; 2; 4 |
Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL; g/100mL |
Pharmaceutical Classes |