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THE FIRST SUN
THE FIRST SUN - 51346-001-01 - (OCTINOXATE, ZINC OXIDE, OCTISALATE, TITANIUM DIOXIDE)
Drug Information of THE FIRST SUN
| Product NDC: | 51346-001 |
| Proprietary Name: | THE FIRST SUN |
| Non Proprietary Name: | OCTINOXATE, ZINC OXIDE, OCTISALATE, TITANIUM DIOXIDE |
| Active Ingredient(s): | 3; 2; 1; 2.61 g/40mL; g/40mL; g/40mL; g/40mL & nbsp; OCTINOXATE, ZINC OXIDE, OCTISALATE, TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of THE FIRST SUN
| Product NDC: | 51346-001 |
| Labeler Name: | NATURE REPUBLIC CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120301 |
Package Information of THE FIRST SUN
| Package NDC: | 51346-001-01 |
| Package Description: | 40 mL in 1 CARTON (51346-001-01) |
NDC Information of THE FIRST SUN
| NDC Code | 51346-001-01 |
| Proprietary Name | THE FIRST SUN |
| Package Description | 40 mL in 1 CARTON (51346-001-01) |
| Product NDC | 51346-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, ZINC OXIDE, OCTISALATE, TITANIUM DIOXIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | NATURE REPUBLIC CO., LTD. |
| Substance Name | OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 3; 2; 1; 2.61 |
| Strength Unit | g/40mL; g/40mL; g/40mL; g/40mL |
| Pharmaceutical Classes |
