Product NDC: | 75909-110 |
Proprietary Name: | ICS PLATINUM |
Non Proprietary Name: | TITANIUM DIOXIDE |
Active Ingredient(s): | 2.69; .67 mL/35mL; mL/35mL & nbsp; TITANIUM DIOXIDE |
Administration Route(s): | CUTANEOUS |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 75909-110 |
Labeler Name: | HANBUL COSMETICS CO., LTD. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100401 |
Package NDC: | 75909-110-01 |
Package Description: | 35 mL in 1 CARTON (75909-110-01) |
NDC Code | 75909-110-01 |
Proprietary Name | ICS PLATINUM |
Package Description | 35 mL in 1 CARTON (75909-110-01) |
Product NDC | 75909-110 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TITANIUM DIOXIDE |
Dosage Form Name | CREAM |
Route Name | CUTANEOUS |
Start Marketing Date | 20100401 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | HANBUL COSMETICS CO., LTD. |
Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 2.69; .67 |
Strength Unit | mL/35mL; mL/35mL |
Pharmaceutical Classes |