United States· US:17518-051_a62bdc56-7a01-4c95-ab20-6098ade5a0b2

3M Avagard

A medicinal product containing chlorhexidine gluconate; alcohol, registered in United States by Solventum US 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…normalised3M AvagardATC—REGISTER NO.US:17518-051_a62bdc56…PACKS LISTED4CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
CHLORHEXIDINE GLUCONATE; ALCOHOL
Manufacturer
Solventum US 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 · 4

  • ndc11
    1751805101
    8 BOTTLE in 1 CASE (17518-051-01) / 500 mL in 1 BOTTLE
  • ndc11
    1751805104
    4 BOTTLE in 1 CASE (17518-051-04) / 1200 mL in 1 BOTTLE
  • ndc11
    17518-051-01
  • ndc11
    17518-051-04

Regulatory notes

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

Same medicine, other countries

Chlorhexidine gluconate; alcohol in 4 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All chlorhexidine gluconate; alcohol products

Authorised across Europe · EMA

The same active substance is authorised in 4 EEA countries. Names it is sold under:

  • Spain · Clorxil, Menalcol Reforzado
  • France · Chlorhexidine Alcoolique Gilbert Healthcare
  • Italy · Clorexifarm Alcolico, Neoxinal Alcolico
  • Netherlands · Chloorhexidinedigluconaat Added Pharma, Chloorhexidinedigluconaat Denteck

Source: European Medicines Agency, Article 57 product data.

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/2cfbb419-80d3-489f-9ec7-de7b276557ab
GET /v1/drugs/2cfbb419-80d3-489f-9ec7-de7b276557ab?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": "TOPICAL",
  "source": "ndc",
  "strength": "8.3; 506.3",
  "substance": "CHLORHEXIDINE GLUCONATE; ALCOHOL",
  "productndc": "17518-051",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "strength_unit": "mg/mL; mg/mL",
  "application_number": "NDA021074",
  "marketing_category": "NDA"
}

See everything about chlorhexidine gluconate; alcohol.

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.