Product NDC: | 43419-374 |
Proprietary Name: | IOPE SUPER VITAL |
Non Proprietary Name: | TITANIUM DIOXIDE, OCTINOXATE, and ZINC OXIDE |
Active Ingredient(s): | 1.08; 1.44; .5292 g/18g; g/18g; g/18g & nbsp; TITANIUM DIOXIDE, OCTINOXATE, and ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43419-374 |
Labeler Name: | AMOREPACIFIC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110201 |
Package NDC: | 43419-374-45 |
Package Description: | 18 g in 1 CONTAINER (43419-374-45) |
NDC Code | 43419-374-45 |
Proprietary Name | IOPE SUPER VITAL |
Package Description | 18 g in 1 CONTAINER (43419-374-45) |
Product NDC | 43419-374 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TITANIUM DIOXIDE, OCTINOXATE, and ZINC OXIDE |
Dosage Form Name | POWDER |
Route Name | TOPICAL |
Start Marketing Date | 20110201 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | AMOREPACIFIC |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 1.08; 1.44; .5292 |
Strength Unit | g/18g; g/18g; g/18g |
Pharmaceutical Classes |