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Koh Gen Do Aqua Foundation
Koh Gen Do Aqua Foundation - 51668-506-01 - (Aqua Foundation)
Drug Information of Koh Gen Do Aqua Foundation
| Product NDC: | 51668-506 |
| Proprietary Name: | Koh Gen Do Aqua Foundation |
| Non Proprietary Name: | Aqua Foundation |
| Active Ingredient(s): | 1.8; 1.38 mL/30mL; mL/30mL & nbsp; Aqua Foundation |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Koh Gen Do Aqua Foundation
| Product NDC: | 51668-506 |
| 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: | 20111103 |
Package Information of Koh Gen Do Aqua Foundation
| Package NDC: | 51668-506-01 |
| Package Description: | 30 mL in 1 CONTAINER (51668-506-01) |
NDC Information of Koh Gen Do Aqua Foundation
| NDC Code | 51668-506-01 |
| Proprietary Name | Koh Gen Do Aqua Foundation |
| Package Description | 30 mL in 1 CONTAINER (51668-506-01) |
| Product NDC | 51668-506 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aqua Foundation |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20111103 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Koh Gen Do USA, Inc |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 1.8; 1.38 |
| Strength Unit | mL/30mL; mL/30mL |
| Pharmaceutical Classes |
