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Timewise Day Solution sunscreen SPF 35 14ml - 51531-8365-0 - (Homosalate,Octisalate,Oxybenzone,Octocrylene,Avobenzone)

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Drug Information of Timewise Day Solution sunscreen SPF 35 14ml

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)

Labeler Information of Timewise Day Solution sunscreen SPF 35 14ml

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 Information of Timewise Day Solution sunscreen SPF 35 14ml

Package NDC: 51531-8365-0
Package Description: 29 mL in 1 BOTTLE, DISPENSING (51531-8365-0)

NDC Information of Timewise Day Solution sunscreen SPF 35 14ml

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

Complete Information of Timewise Day Solution sunscreen SPF 35 14ml


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