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SENSAI SILK BRIGHTENING - 64159-6394-3 - (OCTINOXATE)

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Drug Information of SENSAI SILK BRIGHTENING

Product NDC: 64159-6394
Proprietary Name: SENSAI SILK BRIGHTENING
Non Proprietary Name: OCTINOXATE
Active Ingredient(s): 4    g/100mL & nbsp;   OCTINOXATE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of SENSAI SILK BRIGHTENING

Product NDC: 64159-6394
Labeler Name: KANEBO COSMETICS INC.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20080101

Package Information of SENSAI SILK BRIGHTENING

Package NDC: 64159-6394-3
Package Description: 8 mL in 1 JAR (64159-6394-3)

NDC Information of SENSAI SILK BRIGHTENING

NDC Code 64159-6394-3
Proprietary Name SENSAI SILK BRIGHTENING
Package Description 8 mL in 1 JAR (64159-6394-3)
Product NDC 64159-6394
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20080101
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name KANEBO COSMETICS INC.
Substance Name OCTINOXATE
Strength Number 4
Strength Unit g/100mL
Pharmaceutical Classes

Complete Information of SENSAI SILK BRIGHTENING


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