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Nu Skin Nu Colour - 62839-0805-1 - (Octinoxate, Octisalate, Oxybenzone, and Titanium Dioxide)

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Drug Information of Nu Skin Nu Colour

Product NDC: 62839-0805
Proprietary Name: Nu Skin Nu Colour
Non Proprietary Name: Octinoxate, Octisalate, Oxybenzone, and Titanium Dioxide
Active Ingredient(s): 50; 20; 30; 65.22    g/1000mL; g/1000mL; g/1000mL; g/1000mL & nbsp;   Octinoxate, Octisalate, Oxybenzone, and Titanium Dioxide
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Nu Skin Nu Colour

Product NDC: 62839-0805
Labeler Name: NSE Products, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110103

Package Information of Nu Skin Nu Colour

Package NDC: 62839-0805-1
Package Description: 1 BOTTLE, PUMP in 1 CARTON (62839-0805-1) > 30 mL in 1 BOTTLE, PUMP

NDC Information of Nu Skin Nu Colour

NDC Code 62839-0805-1
Proprietary Name Nu Skin Nu Colour
Package Description 1 BOTTLE, PUMP in 1 CARTON (62839-0805-1) > 30 mL in 1 BOTTLE, PUMP
Product NDC 62839-0805
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate, Octisalate, Oxybenzone, and Titanium Dioxide
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20110103
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name NSE Products, Inc.
Substance Name OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE
Strength Number 50; 20; 30; 65.22
Strength Unit g/1000mL; g/1000mL; g/1000mL; g/1000mL
Pharmaceutical Classes

Complete Information of Nu Skin Nu Colour


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