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Sodium Fluoride and Potassium Nitrate

NDC 69367-318 · Westminster Pharmaceuticals, LLC

Generic nameSodium Fluoride and Potassium Nitrate
Dosage formGEL
RouteDENTAL
Active ingredient(s)SODIUM FLUORIDE, POTASSIUM NITRATE
Strength57.5; 5.8 mg/mL; mg/mL
Marketing categoryUNAPPROVED DRUG OTHER

Packages

69367-318-01 — 1 TUBE in 1 CARTON (69367-318-01) / 100 mL in 1 TUBE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68987-013 — Sodium Fluoride, 68987-014 — Sodium Fluoride, 69261-002 — SODIUM FLUORIDE, 69261-005 — SODIUM FLUORIDE, 69261-006 — SODIUM FLUORIDE, 69261-007 — SODIUM FLUORIDE, 69367-309 — Sodium Fluoride, 69367-310 — Sodium Fluoride, 69367-311 — Sodium Fluoride, 69367-312 — Sodium Fluoride, 69423-745 — Sodium Fluoride, 69423-750 — Sodium Fluoride, 69423-751 — Sodium Fluoride, 69423-762 — Sodium Fluoride, 69423-767 — Sodium Fluoride, 69423-768 — Sodium Fluoride, 69423-769 — Sodium Fluoride, 69423-770 — Sodium Fluoride, 69423-772 — Sodium Fluoride, 69423-773 — Sodium Fluoride, +1099 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels