United States· US:0135-0525_18835f57-a509-2ac6-e063-6394a90a8aaf

Sensodyne

A medicinal product containing potassium nitrate; sodium fluoride, registered in United States by Haleon US Holdings LLC.

US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedSensodyneATC—REGISTER NO.US:0135-0525_18835f57…PACKS LISTED18CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
POTASSIUM NITRATE; SODIUM FLUORIDE
Manufacturer
Haleon US Holdings LLC
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 18

  • ndc11
    0135052503
    2 CARTON in 1 CARTON (0135-0525-03) / 1 TUBE in 1 CARTON / 113 g in 1 TUBE
  • ndc11
    0135052504
    1 TUBE in 1 CARTON (0135-0525-04) / 113 g in 1 TUBE
  • ndc11
    0135052505
    1 TUBE in 1 CARTON (0135-0525-05) / 77 g in 1 TUBE
  • ndc11
    0135052506
    1 TUBE in 1 CARTON (0135-0525-06) / 170 g in 1 TUBE
  • ndc11
    0135052507
    1 TUBE in 1 CARTON (0135-0525-07) / 23 g in 1 TUBE
  • ndc11
    0135052508
    1 TUBE in 1 CARTON (0135-0525-08) / 184 g in 1 TUBE
  • ndc11
    0135052511
    3 CARTON in 1 CARTON (0135-0525-11) / 1 TUBE in 1 CARTON / 184 g in 1 TUBE
  • ndc11
    0135052513
    4 TUBE in 1 CARTON (0135-0525-13) / 184 g in 1 TUBE
  • ndc11
    0135052514
    4 TUBE in 1 CARTON (0135-0525-14) / 184 g in 1 TUBE
  • ndc11
    0135-0525-03
  • ndc11
    0135-0525-04
  • ndc11
    0135-0525-05
  • ndc11
    0135-0525-06
  • ndc11
    0135-0525-07
  • ndc11
    0135-0525-11
  • ndc11
    0135-0525-13
  • ndc11
    0135-0525-14
  • ndc11
    0135-0525-08

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload
GET /v1/drugs/c80cd511-d46f-4370-932f-c9bc78c2cdff
GET /v1/drugs/c80cd511-d46f-4370-932f-c9bc78c2cdff?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "route": "DENTAL",
  "source": "ndc",
  "strength": "50; 1.11",
  "substance": "POTASSIUM NITRATE; SODIUM FLUORIDE",
  "productndc": "0135-0525",
  "dosage_form": "PASTE",
  "dea_schedule": null,
  "strength_unit": "mg/g; mg/g",
  "application_number": "M022",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about potassium nitrate; sodium fluoride.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.