Product NDC: | 51523-023 |
Proprietary Name: | THE FLOWER UV INTENSE PACT |
Non Proprietary Name: | ZINC OXIDE |
Active Ingredient(s): | 1.53; 1.64 g/12g; g/12g & nbsp; ZINC OXIDE |
Administration Route(s): | CUTANEOUS |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51523-023 |
Labeler Name: | THEFACESHOP CO., LTD. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20070301 |
Package NDC: | 51523-023-01 |
Package Description: | 12 g in 1 CARTON (51523-023-01) |
NDC Code | 51523-023-01 |
Proprietary Name | THE FLOWER UV INTENSE PACT |
Package Description | 12 g in 1 CARTON (51523-023-01) |
Product NDC | 51523-023 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ZINC OXIDE |
Dosage Form Name | POWDER |
Route Name | CUTANEOUS |
Start Marketing Date | 20070301 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | THEFACESHOP CO., LTD. |
Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 1.53; 1.64 |
Strength Unit | g/12g; g/12g |
Pharmaceutical Classes |