Product NDC: | 43419-361 |
Proprietary Name: | IOPE SS |
Non Proprietary Name: | OCTINOXATE and ZINC OXIDE |
Active Ingredient(s): | .06; .03 g/g; g/g & nbsp; OCTINOXATE and ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43419-361 |
Labeler Name: | AMOREPACIFIC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20101101 |
Package NDC: | 43419-361-08 |
Package Description: | 14 g in 1 CONTAINER (43419-361-08) |
NDC Code | 43419-361-08 |
Proprietary Name | IOPE SS |
Package Description | 14 g in 1 CONTAINER (43419-361-08) |
Product NDC | 43419-361 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE and ZINC OXIDE |
Dosage Form Name | POWDER |
Route Name | TOPICAL |
Start Marketing Date | 20101101 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | AMOREPACIFIC |
Substance Name | OCTINOXATE; ZINC OXIDE |
Strength Number | .06; .03 |
Strength Unit | g/g; g/g |
Pharmaceutical Classes |