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NATURAL FINISH - 64141-002-01 - (OCTINOXATE, TITANIUM DIOXIDE)

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Drug Information of NATURAL FINISH

Product NDC: 64141-002
Proprietary Name: NATURAL FINISH
Non Proprietary Name: OCTINOXATE, TITANIUM DIOXIDE
Active Ingredient(s): 7.5; 1    mL/100mL; mL/100mL & nbsp;   OCTINOXATE, TITANIUM DIOXIDE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of NATURAL FINISH

Product NDC: 64141-002
Labeler Name: Bobbi Brown Professional Cosmetics Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20071001

Package Information of NATURAL FINISH

Package NDC: 64141-002-01
Package Description: 1 TUBE in 1 CARTON (64141-002-01) > 30 mL in 1 TUBE (64141-002-02)

NDC Information of NATURAL FINISH

NDC Code 64141-002-01
Proprietary Name NATURAL FINISH
Package Description 1 TUBE in 1 CARTON (64141-002-01) > 30 mL in 1 TUBE (64141-002-02)
Product NDC 64141-002
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE, TITANIUM DIOXIDE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20071001
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Bobbi Brown Professional Cosmetics Inc.
Substance Name OCTINOXATE; TITANIUM DIOXIDE
Strength Number 7.5; 1
Strength Unit mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of NATURAL FINISH


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