United States · FDA National Drug Code directory

UNIVERSAL 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
52000-111_42b18d2a-c986-42a0-9f88-9ee8e8b1290b
Product NDC
52000-111
Form
PASTE
Composition / generic term
Sodium Monofluorophosphate
Labeler
Universal Distribution Center LLC
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20200530
Source listing expiry
20261231

Source-listed ingredients

  • SODIUM MONOFLUOROPHOSPHATE — .76 g/100g

These values do not establish equivalence or a dose recommendation.

Packages

  • 181 g in 1 TUBE (52000-111-01) · 52000-111-01

Source and coverage

Open FDA National Drug Code directory

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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UNIVERSAL ANTI-CAVITY FLUORIDE — United States | Molindra Medicines