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Anticavity
Anticavity - 0869-0213-44 - (Sodium Fluoride)
Drug Information of Anticavity
| Product NDC: | 0869-0213 |
| Proprietary Name: | Anticavity |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | .05 kg/100L & nbsp; Sodium Fluoride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | RINSE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Anticavity
| Product NDC: | 0869-0213 |
| Labeler Name: | Vi Jon |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20010621 |
Package Information of Anticavity
| Package NDC: | 0869-0213-44 |
| Package Description: | .532 L in 1 BOTTLE, PLASTIC (0869-0213-44) |
NDC Information of Anticavity
| NDC Code | 0869-0213-44 |
| Proprietary Name | Anticavity |
| Package Description | .532 L in 1 BOTTLE, PLASTIC (0869-0213-44) |
| Product NDC | 0869-0213 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | RINSE |
| Route Name | ORAL |
| Start Marketing Date | 20010621 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Vi Jon |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .05 |
| Strength Unit | kg/100L |
| Pharmaceutical Classes |
