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Sulwhasoo Lumitouch Foundation
Sulwhasoo Lumitouch Foundation - 43419-017-16 - (OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE)
Drug Information of Sulwhasoo Lumitouch Foundation
| Product NDC: | 43419-017 |
| Proprietary Name: | Sulwhasoo Lumitouch Foundation |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Active Ingredient(s): | .352; .4697; .2156 g/11g; g/11g; g/11g & nbsp; OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sulwhasoo Lumitouch Foundation
| Product NDC: | 43419-017 |
| Labeler Name: | AMOREPACIFIC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111223 |
Package Information of Sulwhasoo Lumitouch Foundation
| Package NDC: | 43419-017-16 |
| Package Description: | 11 g in 1 CONTAINER (43419-017-16) |
NDC Information of Sulwhasoo Lumitouch Foundation
| NDC Code | 43419-017-16 |
| Proprietary Name | Sulwhasoo Lumitouch Foundation |
| Package Description | 11 g in 1 CONTAINER (43419-017-16) |
| Product NDC | 43419-017 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20111223 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | AMOREPACIFIC |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | .352; .4697; .2156 |
| Strength Unit | g/11g; g/11g; g/11g |
| Pharmaceutical Classes |
