Product NDC: | 43419-301 |
Proprietary Name: | IOPE RETIGEN ESSENCE DUAL CONCEALER |
Non Proprietary Name: | OCTINOXATE and TITANIUM DIOXIDE |
Active Ingredient(s): | .082; .82 g/4.1g; g/4.1g & nbsp; OCTINOXATE and TITANIUM DIOXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | STICK |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43419-301 |
Labeler Name: | AMOREPACIFIC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110801 |
Package NDC: | 43419-301-05 |
Package Description: | 4.1 g in 1 CYLINDER (43419-301-05) |
NDC Code | 43419-301-05 |
Proprietary Name | IOPE RETIGEN ESSENCE DUAL CONCEALER |
Package Description | 4.1 g in 1 CYLINDER (43419-301-05) |
Product NDC | 43419-301 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE and TITANIUM DIOXIDE |
Dosage Form Name | STICK |
Route Name | TOPICAL |
Start Marketing Date | 20110801 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | AMOREPACIFIC |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
Strength Number | .082; .82 |
Strength Unit | g/4.1g; g/4.1g |
Pharmaceutical Classes |