Product NDC: | 43419-307 |
Proprietary Name: | IOPE RETIGEN MOISTURE FOUNDATION |
Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
Active Ingredient(s): | 1.75; .8715; .343 g/35mL; g/35mL; g/35mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43419-307 |
Labeler Name: | AMOREPACIFIC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110801 |
Package NDC: | 43419-307-03 |
Package Description: | 1 BOTTLE, PUMP in 1 CARTON (43419-307-03) > 35 mL in 1 BOTTLE, PUMP |
NDC Code | 43419-307-03 |
Proprietary Name | IOPE RETIGEN MOISTURE FOUNDATION |
Package Description | 1 BOTTLE, PUMP in 1 CARTON (43419-307-03) > 35 mL in 1 BOTTLE, PUMP |
Product NDC | 43419-307 |
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 | 20110801 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | AMOREPACIFIC |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 1.75; .8715; .343 |
Strength Unit | g/35mL; g/35mL; g/35mL |
Pharmaceutical Classes |