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