| Product NDC: | 51346-039 | 
| Proprietary Name: | UV LOCK FLOWER KIDS AND JUNIOR SUN | 
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE | 
| Active Ingredient(s): | 3.75; 1.05 g/50mL; g/50mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE | 
| Administration Route(s): | TOPICAL | 
| Dosage Form(s): | CREAM | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 51346-039 | 
| Labeler Name: | NATURE REPUBLIC CO., LTD. | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part352 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20120102 | 
| Package NDC: | 51346-039-01 | 
| Package Description: | 50 mL in 1 CARTON (51346-039-01) | 
| NDC Code | 51346-039-01 | 
| Proprietary Name | UV LOCK FLOWER KIDS AND JUNIOR SUN | 
| Package Description | 50 mL in 1 CARTON (51346-039-01) | 
| Product NDC | 51346-039 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE | 
| Dosage Form Name | CREAM | 
| Route Name | TOPICAL | 
| Start Marketing Date | 20120102 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | NATURE REPUBLIC CO., LTD. | 
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE | 
| Strength Number | 3.75; 1.05 | 
| Strength Unit | g/50mL; g/50mL | 
| Pharmaceutical Classes |