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Fluor-a-day
Fluor-a-day - 24338-622-16 - (Sodium fluoride and Xylitol)
Drug Information of Fluor-a-day
| Product NDC: | 24338-622 |
| Proprietary Name: | Fluor-a-day |
| Non Proprietary Name: | Sodium fluoride and Xylitol |
| Active Ingredient(s): | 1; 236.79 mg/1; mg/1 & nbsp; Sodium fluoride and Xylitol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fluor-a-day
| Product NDC: | 24338-622 |
| Labeler Name: | Arbor Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100815 |
Package Information of Fluor-a-day
| Package NDC: | 24338-622-16 |
| Package Description: | 120 TABLET, CHEWABLE in 1 BOTTLE (24338-622-16) |
NDC Information of Fluor-a-day
| NDC Code | 24338-622-16 |
| Proprietary Name | Fluor-a-day |
| Package Description | 120 TABLET, CHEWABLE in 1 BOTTLE (24338-622-16) |
| Product NDC | 24338-622 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium fluoride and Xylitol |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20100815 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Arbor Pharmaceuticals, Inc. |
| Substance Name | SODIUM FLUORIDE; XYLITOL |
| Strength Number | 1; 236.79 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
