| Product NDC: | 43419-004 |
| Proprietary Name: | Sulwhasoo |
| Non Proprietary Name: | OCTINOXATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Active Ingredient(s): | 2.9344; 1.8864; 3.3536; 1.852864; .0431776 g/40mL; g/40mL; g/40mL; g/40mL; g/40mL & nbsp; OCTINOXATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 43419-004 |
| Labeler Name: | AMOREPACIFIC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110501 |
| Package NDC: | 43419-004-02 |
| Package Description: | 40 mL in 1 TUBE (43419-004-02) |
| NDC Code | 43419-004-02 |
| Proprietary Name | Sulwhasoo |
| Package Description | 40 mL in 1 TUBE (43419-004-02) |
| Product NDC | 43419-004 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110501 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | AMOREPACIFIC |
| Substance Name | OCTINOXATE; OCTISALATE; OCTOCRYLENE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 2.9344; 1.8864; 3.3536; 1.852864; .0431776 |
| Strength Unit | g/40mL; g/40mL; g/40mL; g/40mL; g/40mL |
| Pharmaceutical Classes |