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 |