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Mary Kay TimeWise Day Solution Sunscreen SPF 25 - 51531-2326-1 - (octinoxate, octisalate, zinc oxide, oxybenzone,)

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Drug Information of Mary Kay TimeWise Day Solution Sunscreen SPF 25

Product NDC: 51531-2326
Proprietary Name: Mary Kay TimeWise Day Solution Sunscreen SPF 25
Non Proprietary Name: octinoxate, octisalate, zinc oxide, oxybenzone,
Active Ingredient(s): 7.5; 5; 3; 3.88    g/100mL; g/100mL; g/100mL; g/100mL & nbsp;   octinoxate, octisalate, zinc oxide, oxybenzone,
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Mary Kay TimeWise Day Solution Sunscreen SPF 25

Product NDC: 51531-2326
Labeler Name: Mary Kay Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20051216

Package Information of Mary Kay TimeWise Day Solution Sunscreen SPF 25

Package NDC: 51531-2326-1
Package Description: 1 BOTTLE, PUMP in 1 CARTON (51531-2326-1) > 29 mL in 1 BOTTLE, PUMP

NDC Information of Mary Kay TimeWise Day Solution Sunscreen SPF 25

NDC Code 51531-2326-1
Proprietary Name Mary Kay TimeWise Day Solution Sunscreen SPF 25
Package Description 1 BOTTLE, PUMP in 1 CARTON (51531-2326-1) > 29 mL in 1 BOTTLE, PUMP
Product NDC 51531-2326
Product Type Name HUMAN OTC DRUG
Non Proprietary Name octinoxate, octisalate, zinc oxide, oxybenzone,
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20051216
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Mary Kay Inc.
Substance Name OCTINOXATE; OCTISALATE; OXYBENZONE; ZINC OXIDE
Strength Number 7.5; 5; 3; 3.88
Strength Unit g/100mL; g/100mL; g/100mL; g/100mL
Pharmaceutical Classes

Complete Information of Mary Kay TimeWise Day Solution Sunscreen SPF 25


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