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fluorodine ULTRA active Fluoride Anticavity
fluorodine ULTRA active Fluoride Anticavity - 22912-002-00 - (SODIUM FLUORIDE)
Drug Information of fluorodine ULTRA active Fluoride Anticavity
| Product NDC: | 22912-002 |
| Proprietary Name: | fluorodine ULTRA active Fluoride Anticavity |
| Non Proprietary Name: | SODIUM FLUORIDE |
| Active Ingredient(s): | .24 g/100g & nbsp; SODIUM FLUORIDE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of fluorodine ULTRA active Fluoride Anticavity
| Product NDC: | 22912-002 |
| Labeler Name: | Multibrands International Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130327 |
Package Information of fluorodine ULTRA active Fluoride Anticavity
| Package NDC: | 22912-002-00 |
| Package Description: | 1 TUBE in 1 PACKAGE (22912-002-00) > 132 g in 1 TUBE |
NDC Information of fluorodine ULTRA active Fluoride Anticavity
| NDC Code | 22912-002-00 |
| Proprietary Name | fluorodine ULTRA active Fluoride Anticavity |
| Package Description | 1 TUBE in 1 PACKAGE (22912-002-00) > 132 g in 1 TUBE |
| Product NDC | 22912-002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM FLUORIDE |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20130327 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Multibrands International Ltd |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .24 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
