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IOPE BRIGHTGEN - 43419-330-18 - (OXYBENZONE, OCTINOXATE, OCTISALATE, HOMOSALATE, OCTOCRYLENE, and TITANIUM DIOXIDE)

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Drug Information of IOPE BRIGHTGEN

Product NDC: 43419-330
Proprietary Name: IOPE BRIGHTGEN
Non Proprietary Name: OXYBENZONE, OCTINOXATE, OCTISALATE, HOMOSALATE, OCTOCRYLENE, and TITANIUM DIOXIDE
Active Ingredient(s): 3.18; 4.452; 2.862; 3.18; 2.862; 3.3072    g/60mL; g/60mL; g/60mL; g/60mL; g/60mL; g/60mL & nbsp;   OXYBENZONE, OCTINOXATE, OCTISALATE, HOMOSALATE, OCTOCRYLENE, and TITANIUM DIOXIDE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of IOPE BRIGHTGEN

Product NDC: 43419-330
Labeler Name: AMOREPACIFIC
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120824

Package Information of IOPE BRIGHTGEN

Package NDC: 43419-330-18
Package Description: 1 TUBE in 1 CARTON (43419-330-18) > 60 mL in 1 TUBE

NDC Information of IOPE BRIGHTGEN

NDC Code 43419-330-18
Proprietary Name IOPE BRIGHTGEN
Package Description 1 TUBE in 1 CARTON (43419-330-18) > 60 mL in 1 TUBE
Product NDC 43419-330
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OXYBENZONE, OCTINOXATE, OCTISALATE, HOMOSALATE, OCTOCRYLENE, and TITANIUM DIOXIDE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20120824
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name AMOREPACIFIC
Substance Name HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE; TITANIUM DIOXIDE
Strength Number 3.18; 4.452; 2.862; 3.18; 2.862; 3.3072
Strength Unit g/60mL; g/60mL; g/60mL; g/60mL; g/60mL; g/60mL
Pharmaceutical Classes

Complete Information of IOPE BRIGHTGEN


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