| Product NDC: | 51668-201 |
| Proprietary Name: | Koh Gen Do Maifanshi UV Face Powder |
| Non Proprietary Name: | titanium dioxide |
| Active Ingredient(s): | .9558 g/12g & nbsp; titanium dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51668-201 |
| Labeler Name: | Koh Gen Do USA, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110825 |
| Package NDC: | 51668-201-06 |
| Package Description: | 12 g in 1 CONTAINER (51668-201-06) |
| NDC Code | 51668-201-06 |
| Proprietary Name | Koh Gen Do Maifanshi UV Face Powder |
| Package Description | 12 g in 1 CONTAINER (51668-201-06) |
| Product NDC | 51668-201 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | titanium dioxide |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20110825 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Koh Gen Do USA, Inc |
| Substance Name | TITANIUM DIOXIDE |
| Strength Number | .9558 |
| Strength Unit | g/12g |
| Pharmaceutical Classes |