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Anticavity
Anticavity - 51009-001-16 - (Sodium Fluoride)
Drug Information of Anticavity
| Product NDC: | 51009-001 |
| Proprietary Name: | Anticavity |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | .46277 mg/mL & nbsp; Sodium Fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | RINSE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Anticavity
| Product NDC: | 51009-001 |
| Labeler Name: | Tom's of Maine, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100830 |
Package Information of Anticavity
| Package NDC: | 51009-001-16 |
| Package Description: | 473 mL in 1 BOTTLE, PLASTIC (51009-001-16) |
NDC Information of Anticavity
| NDC Code | 51009-001-16 |
| Proprietary Name | Anticavity |
| Package Description | 473 mL in 1 BOTTLE, PLASTIC (51009-001-16) |
| Product NDC | 51009-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | RINSE |
| Route Name | DENTAL |
| Start Marketing Date | 20100830 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Tom's of Maine, Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .46277 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
