Product NDC: | 51621-012 |
Proprietary Name: | Gowoonsesang Medi UV Block Suncream |
Non Proprietary Name: | ZINC OXIDE |
Active Ingredient(s): | 1.49; 2.88 mL/60mL; mL/60mL & nbsp; ZINC OXIDE |
Administration Route(s): | CUTANEOUS |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51621-012 |
Labeler Name: | GOWOONSESANG COSMETICS CO., LTD. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090601 |
Package NDC: | 51621-012-01 |
Package Description: | 60 mL in 1 CARTON (51621-012-01) |
NDC Code | 51621-012-01 |
Proprietary Name | Gowoonsesang Medi UV Block Suncream |
Package Description | 60 mL in 1 CARTON (51621-012-01) |
Product NDC | 51621-012 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ZINC OXIDE |
Dosage Form Name | CREAM |
Route Name | CUTANEOUS |
Start Marketing Date | 20090601 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | GOWOONSESANG COSMETICS CO., LTD. |
Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 1.49; 2.88 |
Strength Unit | mL/60mL; mL/60mL |
Pharmaceutical Classes |