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PAUL and JOE - 42908-057-00 - (OCTINOXATE and TITANIUM DIOXIDE)

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Drug Information of PAUL and JOE

Product NDC: 42908-057
Proprietary Name: PAUL and JOE
Non Proprietary Name: OCTINOXATE and TITANIUM DIOXIDE
Active Ingredient(s): 1.5; 2.94    g/30mL; g/30mL & nbsp;   OCTINOXATE and TITANIUM DIOXIDE
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of PAUL and JOE

Product NDC: 42908-057
Labeler Name: Albion Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110301

Package Information of PAUL and JOE

Package NDC: 42908-057-00
Package Description: 1 BOTTLE, GLASS in 1 BOX (42908-057-00) > 30 mL in 1 BOTTLE, GLASS

NDC Information of PAUL and JOE

NDC Code 42908-057-00
Proprietary Name PAUL and JOE
Package Description 1 BOTTLE, GLASS in 1 BOX (42908-057-00) > 30 mL in 1 BOTTLE, GLASS
Product NDC 42908-057
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE and TITANIUM DIOXIDE
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20110301
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Albion Co., Ltd.
Substance Name OCTINOXATE; TITANIUM DIOXIDE
Strength Number 1.5; 2.94
Strength Unit g/30mL; g/30mL
Pharmaceutical Classes

Complete Information of PAUL and JOE


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