Product NDC: | 51668-404 |
Proprietary Name: | Koh Gen DoTriple Lighting |
Non Proprietary Name: | Titanium Dioxide |
Active Ingredient(s): | 13.1 g/100g & nbsp; Titanium Dioxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51668-404 |
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: | 20110322 |
Package NDC: | 51668-404-04 |
Package Description: | 9 g in 1 CONTAINER (51668-404-04) |
NDC Code | 51668-404-04 |
Proprietary Name | Koh Gen DoTriple Lighting |
Package Description | 9 g in 1 CONTAINER (51668-404-04) |
Product NDC | 51668-404 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Titanium Dioxide |
Dosage Form Name | POWDER |
Route Name | TOPICAL |
Start Marketing Date | 20110322 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Koh Gen Do USA, Inc |
Substance Name | TITANIUM DIOXIDE |
Strength Number | 13.1 |
Strength Unit | g/100g |
Pharmaceutical Classes |