UNIVERSAL ADVANCED WHITENING ANTI-CAVITY FLUORIDE
NDC 52000-112 · Universal Distribution Center LLC
Packages
52000-112-01 — 181 g in 1 TUBE (52000-112-01)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
51009-859 — Sodium monofluorophosphate, 51009-860 — Sodium monofluorophosphate, 51009-902 — Sodium Monofluorophosphate, 51009-910 — SODIUM MONOFLUOROPHOSPHATE, 51009-911 — SODIUM MONOFLUOROPHOSPHATE, 51009-912 — SODIUM MONOFLUOROPHOSPHATE, 51824-067 — Sodium Monofluorophosphate, 52000-107 — Sodium Monofluorophosphate, 52000-108 — Sodium Monofluorophosphate, 52000-111 — Sodium Monofluorophosphate, 52257-1370 — Sodium Monofluorophosphate, Sodium Fluoride, 52257-1380 — Sodium Monofluorophosphate, Sodium Fluoride, 52410-9005 — Sodium monofluorophosphate, 53238-002 — POTASSIUM NITRATE, SODIUM MONOFLUOROPHOSPHATE, 53238-003 — SODIUM MONOFLUOROPHOSPHATE, 53247-129 — Sodium Monofluorophosphate, 53329-083 — Sodium Monofluorophosphate, 53567-0030 — Sodium Monofluorophosphate, 53567-0031 — Sodium Monofluorophosphate, 53567-0032 — Sodium Monofluorophosphate, +132 more
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