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Sandy Beige - 68828-079-01 - (Titanium Dioxide, Octinoxate/EthylhexylMehtoxycinnamate)

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Drug Information of Sandy Beige

Product NDC: 68828-079
Proprietary Name: Sandy Beige
Non Proprietary Name: Titanium Dioxide, Octinoxate/EthylhexylMehtoxycinnamate
Active Ingredient(s): 2.5; 8    mL/100mL; mL/100mL & nbsp;   Titanium Dioxide, Octinoxate/EthylhexylMehtoxycinnamate
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sandy Beige

Product NDC: 68828-079
Labeler Name: Jafra Cosmetics International Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120516

Package Information of Sandy Beige

Package NDC: 68828-079-01
Package Description: 1 BOTTLE, GLASS in 1 BOX (68828-079-01) > 30 mL in 1 BOTTLE, GLASS

NDC Information of Sandy Beige

NDC Code 68828-079-01
Proprietary Name Sandy Beige
Package Description 1 BOTTLE, GLASS in 1 BOX (68828-079-01) > 30 mL in 1 BOTTLE, GLASS
Product NDC 68828-079
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Titanium Dioxide, Octinoxate/EthylhexylMehtoxycinnamate
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20120516
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Jafra Cosmetics International Inc
Substance Name OCTINOXATE; TITANIUM DIOXIDE
Strength Number 2.5; 8
Strength Unit mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of Sandy Beige


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