Product NDC: | 43419-510 |
Proprietary Name: | AMOREPACIFIC |
Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
Active Ingredient(s): | 1.5; 1.245; .294 mL/30mL; mL/30mL; mL/30mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43419-510 |
Labeler Name: | AMOREPACIFIC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110601 |
Package NDC: | 43419-510-11 |
Package Description: | 1 mL in 1 POUCH (43419-510-11) |
NDC Code | 43419-510-11 |
Proprietary Name | AMOREPACIFIC |
Package Description | 1 mL in 1 POUCH (43419-510-11) |
Product NDC | 43419-510 |
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 | 20110601 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | AMOREPACIFIC |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 1.5; 1.245; .294 |
Strength Unit | mL/30mL; mL/30mL; mL/30mL |
Pharmaceutical Classes |