United States · FDA National Drug Code directory
PRO Gel 5000 Mint
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 61578-215_424ae751-1f8e-4e67-ba2e-b368d447053e
- Product NDC
- 61578-215
- Form
- GEL, DENTIFRICE
- Composition / generic term
- Sodium fluoride
- Labeler
- DENTAL ALLIANCE HOLDINGS LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20220510
- Source listing expiry
- 20261231
Source-listed ingredients
- SODIUM FLUORIDE — 5000 ug/g
These values do not establish equivalence or a dose recommendation.
Packages
- 68 g in 1 TUBE, WITH APPLICATOR (61578-215-01) · 61578-215-01
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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