| 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 |