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Sulwhasoo Lumitouch
Sulwhasoo Lumitouch - 43419-717-18 - (OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE)
Drug Information of Sulwhasoo Lumitouch
| Product NDC: | 43419-717 |
| Proprietary Name: | Sulwhasoo Lumitouch |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Active Ingredient(s): | .9; .82; .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) |
Labeler Information of Sulwhasoo Lumitouch
| Product NDC: | 43419-717 |
| Labeler Name: | AMOREPACIFIC CO. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100901 |
Package Information of Sulwhasoo Lumitouch
| Package NDC: | 43419-717-18 |
| Package Description: | 30 mL in 1 BOTTLE (43419-717-18) |
NDC Information of Sulwhasoo Lumitouch
| NDC Code | 43419-717-18 |
| Proprietary Name | Sulwhasoo Lumitouch |
| Package Description | 30 mL in 1 BOTTLE (43419-717-18) |
| Product NDC | 43419-717 |
| 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 | 20100901 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | AMOREPACIFIC CO. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | .9; .82; .294 |
| Strength Unit | mL/30mL; mL/30mL; mL/30mL |
| Pharmaceutical Classes |
