Home
>
National Drug Code (NDC)
>
Canker Complete
Canker Complete - 44717-890-02 - (Menthol)
Drug Information of Canker Complete
| Product NDC: | 44717-890 |
| Proprietary Name: | Canker Complete |
| Non Proprietary Name: | Menthol |
| Active Ingredient(s): | .5 g/100g & nbsp; Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Canker Complete
| Product NDC: | 44717-890 |
| Labeler Name: | Wasatch Product Development |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101011 |
Package Information of Canker Complete
| Package NDC: | 44717-890-02 |
| Package Description: | 1 TUBE in 1 BOX (44717-890-02) > 6 g in 1 TUBE (44717-890-01) |
NDC Information of Canker Complete
| NDC Code | 44717-890-02 |
| Proprietary Name | Canker Complete |
| Package Description | 1 TUBE in 1 BOX (44717-890-02) > 6 g in 1 TUBE (44717-890-01) |
| Product NDC | 44717-890 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20101011 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Wasatch Product Development |
| Substance Name | MENTHOL |
| Strength Number | .5 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
