| Product NDC: | 51346-211 |
| Proprietary Name: | UV LOCK FLOWER SUN |
| Non Proprietary Name: | OCTINOXATE, Titanium Dioxide, OCTISALATE |
| Active Ingredient(s): | 2.21; 1.47; 2.18 mg/150mL; mg/150mL; mg/150mL & nbsp; OCTINOXATE, Titanium Dioxide, OCTISALATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51346-211 |
| Labeler Name: | NATURE REPUBLIC CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130201 |
| Package NDC: | 51346-211-01 |
| Package Description: | 150 mL in 1 CARTON (51346-211-01) |
| NDC Code | 51346-211-01 |
| Proprietary Name | UV LOCK FLOWER SUN |
| Package Description | 150 mL in 1 CARTON (51346-211-01) |
| Product NDC | 51346-211 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, Titanium Dioxide, OCTISALATE |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20130201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | NATURE REPUBLIC CO., LTD. |
| Substance Name | OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE |
| Strength Number | 2.21; 1.47; 2.18 |
| Strength Unit | mg/150mL; mg/150mL; mg/150mL |
| Pharmaceutical Classes |