| 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 |