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IQQU Advance Sunscreen - 50403-999-92 - (Dimethicone and Butyl Methoxydibenzoylmethane and Titanium Dioxide and Octyl Methoxycinnamate)

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Drug Information of IQQU Advance Sunscreen

Product NDC: 50403-999
Proprietary Name: IQQU Advance Sunscreen
Non Proprietary Name: Dimethicone and Butyl Methoxydibenzoylmethane and Titanium Dioxide and Octyl Methoxycinnamate
Active Ingredient(s): 22; 25; 50; 40    g/mL; g/mL; g/mL; g/mL & nbsp;   Dimethicone and Butyl Methoxydibenzoylmethane and Titanium Dioxide and Octyl Methoxycinnamate
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of IQQU Advance Sunscreen

Product NDC: 50403-999
Labeler Name: IQQU USA Co.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100125

Package Information of IQQU Advance Sunscreen

Package NDC: 50403-999-92
Package Description: 1 TUBE in 1 CARTON (50403-999-92) > 30 mL in 1 TUBE

NDC Information of IQQU Advance Sunscreen

NDC Code 50403-999-92
Proprietary Name IQQU Advance Sunscreen
Package Description 1 TUBE in 1 CARTON (50403-999-92) > 30 mL in 1 TUBE
Product NDC 50403-999
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dimethicone and Butyl Methoxydibenzoylmethane and Titanium Dioxide and Octyl Methoxycinnamate
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20100125
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name IQQU USA Co.
Substance Name AVOBENZONE; DIMETHICONE; OCTINOXATE; TITANIUM DIOXIDE
Strength Number 22; 25; 50; 40
Strength Unit g/mL; g/mL; g/mL; g/mL
Pharmaceutical Classes

Complete Information of IQQU Advance Sunscreen


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