| 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 |