| Product NDC: | 51523-020 |
| Proprietary Name: | NATURAL SUN AQ POWER LONG LASTING SUN |
| Non Proprietary Name: | ZINC OXIDE |
| Active Ingredient(s): | 2.25; 5.5 mL/50mL; mL/50mL & nbsp; ZINC OXIDE |
| Administration Route(s): | CUTANEOUS |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51523-020 |
| Labeler Name: | THEFACESHOP CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100401 |
| Package NDC: | 51523-020-01 |
| Package Description: | 50 mL in 1 CARTON (51523-020-01) |
| NDC Code | 51523-020-01 |
| Proprietary Name | NATURAL SUN AQ POWER LONG LASTING SUN |
| Package Description | 50 mL in 1 CARTON (51523-020-01) |
| Product NDC | 51523-020 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ZINC OXIDE |
| Dosage Form Name | CREAM |
| Route Name | CUTANEOUS |
| Start Marketing Date | 20100401 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | THEFACESHOP CO., LTD. |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 2.25; 5.5 |
| Strength Unit | mL/50mL; mL/50mL |
| Pharmaceutical Classes |