Skip to main content

PureLife APF

NDC 68987-014 · PureLife Dental

Generic nameSodium Fluoride
Dosage formGEL
RouteDENTAL
Active ingredient(s)SODIUM FLUORIDE
Strength5.6 g/454g
Marketing categoryUNAPPROVED DRUG OTHER

Packages

68987-014-15 — 454 g in 1 BOTTLE, PLASTIC (68987-014-15)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68400-122 — Sodium Fluoride, 68400-135 — Sodium Fluoride, 68400-136 — Sodium Fluoride, 68400-313 — Sodium Fluoride, 68400-324 — Sodium Fluoride, 68599-9573 — Sodium Fluoride, 68987-010 — Sodium Fluoride, 68987-011 — Sodium Fluoride, 68987-012 — Sodium Fluoride, 68987-013 — 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, 69367-318 — Sodium Fluoride and Potassium Nitrate, 69423-745 — Sodium Fluoride, +1070 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