United States · FDA National Drug Code directory
UNIVERSAL SENSITIVE ANTI-CAVITY FLUORIDE
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
- 52000-109_1199f2f8-98e4-4b76-9be9-3b921495a3c3
- Product NDC
- 52000-109
- Form
- PASTE
- Composition / generic term
- potassium nitrate and sodium fluoride
- Labeler
- Universal Distribution Center LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20200520
- Source listing expiry
- 20261231
Source-listed ingredients
- POTASSIUM NITRATE — 5 g/100g
- SODIUM FLUORIDE — .15 g/100g
These values do not establish equivalence or a dose recommendation.
Packages
- 122 g in 1 TUBE (52000-109-01) · 52000-109-01
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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