Product NDC: | 43419-398 |
Proprietary Name: | IOPE MILD CLINIC SUN PROTECTOR |
Non Proprietary Name: | TITANIUM DIOXIDE and ZINC OXIDE |
Active Ingredient(s): | 2.22; 4.53 mL/60mL; mL/60mL & nbsp; TITANIUM DIOXIDE and ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43419-398 |
Labeler Name: | AMOREPACIFIC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110516 |
Package NDC: | 43419-398-98 |
Package Description: | 60 mL in 1 TUBE (43419-398-98) |
NDC Code | 43419-398-98 |
Proprietary Name | IOPE MILD CLINIC SUN PROTECTOR |
Package Description | 60 mL in 1 TUBE (43419-398-98) |
Product NDC | 43419-398 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TITANIUM DIOXIDE and ZINC OXIDE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20110516 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | AMOREPACIFIC |
Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 2.22; 4.53 |
Strength Unit | mL/60mL; mL/60mL |
Pharmaceutical Classes |