United States · FDA National Drug Code directory
SF
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
- 60258-151_58792242-e746-40e6-b549-83cd5f2b7ac5
- Product NDC
- 60258-151
- Form
- GEL
- Composition / generic term
- 1.1% Sodium Fluoride
- Labeler
- Cypress Pharmaceutical, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 19991201
- Source listing expiry
- 20261231
Source-listed ingredients
- SODIUM FLUORIDE — 11 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (60258-151-01) / 56 g in 1 TUBE · 60258-151-01
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.
Browse United States records →