| Product NDC: | 51523-024 |
| Proprietary Name: | THE FLOWER UV INTENSE PACT |
| Non Proprietary Name: | ZINC OXIDE |
| Active Ingredient(s): | 1.54; 1.65 g/12g; g/12g & nbsp; ZINC OXIDE |
| Administration Route(s): | CUTANEOUS |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51523-024 |
| 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: | 51523-024-01 |
| Package Description: | 12 g in 1 CARTON (51523-024-01) |
| NDC Code | 51523-024-01 |
| Proprietary Name | THE FLOWER UV INTENSE PACT |
| Package Description | 12 g in 1 CARTON (51523-024-01) |
| Product NDC | 51523-024 |
| 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 | 1.54; 1.65 |
| Strength Unit | g/12g; g/12g |
| Pharmaceutical Classes |