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SULWHASOO SNOWISE BRIGHTENING BB BASE
SULWHASOO SNOWISE BRIGHTENING BB BASE - 43419-005-14 - (OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE)
Drug Information of SULWHASOO SNOWISE BRIGHTENING BB BASE
| Product NDC: | 43419-005 |
| Proprietary Name: | SULWHASOO SNOWISE BRIGHTENING BB BASE |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Active Ingredient(s): | 2.1; .996; 2.352 g/30mL; g/30mL; g/30mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SULWHASOO SNOWISE BRIGHTENING BB BASE
| Product NDC: | 43419-005 |
| Labeler Name: | AMOREPACIFIC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111005 |
Package Information of SULWHASOO SNOWISE BRIGHTENING BB BASE
| Package NDC: | 43419-005-14 |
| Package Description: | 5 mL in 1 TUBE (43419-005-14) |
NDC Information of SULWHASOO SNOWISE BRIGHTENING BB BASE
| NDC Code | 43419-005-14 |
| Proprietary Name | SULWHASOO SNOWISE BRIGHTENING BB BASE |
| Package Description | 5 mL in 1 TUBE (43419-005-14) |
| Product NDC | 43419-005 |
| 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 | 20111005 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | AMOREPACIFIC |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 2.1; .996; 2.352 |
| Strength Unit | g/30mL; g/30mL; g/30mL |
| Pharmaceutical Classes |
