Product NDC: | 43419-314 |
Proprietary Name: | IOPE RETIGEN SMOOTHING PACT |
Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
Active Ingredient(s): | .84; .86912; .4116 g/14g; g/14g; g/14g & nbsp; OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43419-314 |
Labeler Name: | AMOREPACIFIC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110801 |
Package NDC: | 43419-314-06 |
Package Description: | 14 g in 1 CONTAINER (43419-314-06) |
NDC Code | 43419-314-06 |
Proprietary Name | IOPE RETIGEN SMOOTHING PACT |
Package Description | 14 g in 1 CONTAINER (43419-314-06) |
Product NDC | 43419-314 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
Dosage Form Name | POWDER |
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 | .84; .86912; .4116 |
Strength Unit | g/14g; g/14g; g/14g |
Pharmaceutical Classes |