Product NDC: | 43419-339 |
Proprietary Name: | IOPE B.B. |
Non Proprietary Name: | Octinoxate and TITANIUM DIOXIDE |
Active Ingredient(s): | 2; 1.2 mL/40mL; mL/40mL & nbsp; Octinoxate and TITANIUM DIOXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43419-339 |
Labeler Name: | AMOREPACIFIC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100801 |
Package NDC: | 43419-339-66 |
Package Description: | 40 mL in 1 BOTTLE (43419-339-66) |
NDC Code | 43419-339-66 |
Proprietary Name | IOPE B.B. |
Package Description | 40 mL in 1 BOTTLE (43419-339-66) |
Product NDC | 43419-339 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate and TITANIUM DIOXIDE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20100801 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | AMOREPACIFIC |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
Strength Number | 2; 1.2 |
Strength Unit | mL/40mL; mL/40mL |
Pharmaceutical Classes |