Home
>
National Drug Code (NDC)
>
IOPE RETIGEN LUMINOUS BASE
IOPE RETIGEN LUMINOUS BASE - 43419-306-03 - (OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE)
Drug Information of IOPE RETIGEN LUMINOUS BASE
| Product NDC: | 43419-306 |
| Proprietary Name: | IOPE RETIGEN LUMINOUS BASE |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Active Ingredient(s): | 2.45; .581; .686 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) |
Labeler Information of IOPE RETIGEN LUMINOUS BASE
| Product NDC: | 43419-306 |
| Labeler Name: | AMOREPACIFIC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110801 |
Package Information of IOPE RETIGEN LUMINOUS BASE
| Package NDC: | 43419-306-03 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (43419-306-03) > 35 mL in 1 BOTTLE, PUMP |
NDC Information of IOPE RETIGEN LUMINOUS BASE
| NDC Code | 43419-306-03 |
| Proprietary Name | IOPE RETIGEN LUMINOUS BASE |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (43419-306-03) > 35 mL in 1 BOTTLE, PUMP |
| Product NDC | 43419-306 |
| 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 | 2.45; .581; .686 |
| Strength Unit | g/35mL; g/35mL; g/35mL |
| Pharmaceutical Classes |
