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 |