| Product NDC: | 51346-209 | 
| Proprietary Name: | UV LOCK FLOWER 3 PROOF SUN | 
| Non Proprietary Name: | OCTINOXATE, OCTISALATE, Zinc Oxide, Titanium Dioxide | 
| Active Ingredient(s): | 3.75; 2.5; 1.45; 2.45 mg/50mL; mg/50mL; mg/50mL; mg/50mL & nbsp; OCTINOXATE, OCTISALATE, Zinc Oxide, Titanium Dioxide | 
| Administration Route(s): | TOPICAL | 
| Dosage Form(s): | CREAM | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 51346-209 | 
| 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: | 51346-209-01 | 
| Package Description: | 50 mL in 1 CARTON (51346-209-01) | 
| NDC Code | 51346-209-01 | 
| Proprietary Name | UV LOCK FLOWER 3 PROOF SUN | 
| Package Description | 50 mL in 1 CARTON (51346-209-01) | 
| Product NDC | 51346-209 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | OCTINOXATE, OCTISALATE, Zinc Oxide, Titanium Dioxide | 
| Dosage Form Name | CREAM | 
| 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; ZINC OXIDE | 
| Strength Number | 3.75; 2.5; 1.45; 2.45 | 
| Strength Unit | mg/50mL; mg/50mL; mg/50mL; mg/50mL | 
| Pharmaceutical Classes |