Product NDC: | 43419-358 |
Proprietary Name: | IOPE SS |
Non Proprietary Name: | Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE |
Active Ingredient(s): | .05; .03; .01 mL/mL; mL/mL; mL/mL & nbsp; Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43419-358 |
Labeler Name: | AMOREPACIFIC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20101101 |
Package NDC: | 43419-358-05 |
Package Description: | 35 mL in 1 BOTTLE (43419-358-05) |
NDC Code | 43419-358-05 |
Proprietary Name | IOPE SS |
Package Description | 35 mL in 1 BOTTLE (43419-358-05) |
Product NDC | 43419-358 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20101101 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | AMOREPACIFIC |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | .05; .03; .01 |
Strength Unit | mL/mL; mL/mL; mL/mL |
Pharmaceutical Classes |