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CACTUS WHITENING SUN - 76214-032-01 - (OCTINOXATE)

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Drug Information of CACTUS WHITENING SUN

Product NDC: 76214-032
Proprietary Name: CACTUS WHITENING SUN
Non Proprietary Name: OCTINOXATE
Active Ingredient(s): 4.9; 3.5; .65    mL/70mL; mL/70mL; mL/70mL & nbsp;   OCTINOXATE
Administration Route(s): CUTANEOUS
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of CACTUS WHITENING SUN

Product NDC: 76214-032
Labeler Name: SKINFOOD CO., LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110301

Package Information of CACTUS WHITENING SUN

Package NDC: 76214-032-01
Package Description: 70 mL in 1 BOTTLE (76214-032-01)

NDC Information of CACTUS WHITENING SUN

NDC Code 76214-032-01
Proprietary Name CACTUS WHITENING SUN
Package Description 70 mL in 1 BOTTLE (76214-032-01)
Product NDC 76214-032
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE
Dosage Form Name LOTION
Route Name CUTANEOUS
Start Marketing Date 20110301
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name SKINFOOD CO., LTD.
Substance Name OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE
Strength Number 4.9; 3.5; .65
Strength Unit mL/70mL; mL/70mL; mL/70mL
Pharmaceutical Classes

Complete Information of CACTUS WHITENING SUN


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