Product NDC: | 51531-8365 |
Proprietary Name: | Timewise Day Solution sunscreen SPF 35 14ml |
Non Proprietary Name: | Homosalate,Octisalate,Oxybenzone,Octocrylene,Avobenzone |
Active Ingredient(s): | .28; 1.4; .7; .28; .56 mL/14mL; mL/14mL; mL/14mL; mL/14mL; mL/14mL & nbsp; Homosalate,Octisalate,Oxybenzone,Octocrylene,Avobenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51531-8365 |
Labeler Name: | Mary Kay Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120301 |
Package NDC: | 51531-8365-0 |
Package Description: | 29 mL in 1 BOTTLE, DISPENSING (51531-8365-0) |
NDC Code | 51531-8365-0 |
Proprietary Name | Timewise Day Solution sunscreen SPF 35 14ml |
Package Description | 29 mL in 1 BOTTLE, DISPENSING (51531-8365-0) |
Product NDC | 51531-8365 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Homosalate,Octisalate,Oxybenzone,Octocrylene,Avobenzone |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120301 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Mary Kay Inc. |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | .28; 1.4; .7; .28; .56 |
Strength Unit | mL/14mL; mL/14mL; mL/14mL; mL/14mL; mL/14mL |
Pharmaceutical Classes |