| Product NDC: | 43419-371 |
| Proprietary Name: | IOPE SUPER VITAL |
| Non Proprietary Name: | TITANIUM DIOXIDE and OCTINOXATE |
| Active Ingredient(s): | 1.75; .35 mL/35mL; mL/35mL & nbsp; TITANIUM DIOXIDE and OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 43419-371 |
| Labeler Name: | AMOREPACIFIC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110201 |
| Package NDC: | 43419-371-42 |
| Package Description: | 35 mL in 1 CONTAINER (43419-371-42) |
| NDC Code | 43419-371-42 |
| Proprietary Name | IOPE SUPER VITAL |
| Package Description | 35 mL in 1 CONTAINER (43419-371-42) |
| Product NDC | 43419-371 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE and OCTINOXATE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | AMOREPACIFIC |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 1.75; .35 |
| Strength Unit | mL/35mL; mL/35mL |
| Pharmaceutical Classes |