United States · FDA National Drug Code directory

Sodium Monofluorophosphate

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
67777-181_1c58c582-92e0-4533-e063-6394a90a9fe5
Product NDC
67777-181
Form
PASTE
Composition / generic term
White Toothpaste
Labeler
Dynarex Corporation
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20240716
Source listing expiry
20261231

Source-listed ingredients

  • SODIUM MONOFLUOROPHOSPHATE — 760 mg/g

These values do not establish equivalence or a dose recommendation.

Packages

  • 144 TUBE in 1 CASE (67777-181-02) / 42.5 g in 1 TUBE (67777-181-01) · 67777-181-02
  • 144 TUBE in 1 CASE (67777-181-04) / 78 g in 1 TUBE (67777-181-03) · 67777-181-04
  • 60 BOX in 1 CASE (67777-181-07) / 1 TUBE in 1 BOX (67777-181-06) / 130 g in 1 TUBE (67777-181-05) · 67777-181-07
  • 720 BOX in 1 CASE (67777-181-10) / 144 TUBE in 1 BOX (67777-181-09) / 24 g in 1 TUBE (67777-181-08) · 67777-181-10
  • 720 BOX in 1 CASE (67777-181-13) / 144 TUBE in 1 BOX (67777-181-12) / 17 g in 1 TUBE (67777-181-11) · 67777-181-13

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.

Browse United States records →