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Brand-name over-the-counter medicine

Avagard

Generic name: Alcohol and chlorhexidine gluconate

FDA application holder: Solventum

Official data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the NDC Directory, Drugs@FDA, the official labels and recall reports; pharmacy costs come from the Centers for Medicare & Medicaid Services (CMS). Each fact shows its source and date.

This page is not medical advice. Read the label on your package, and ask a pharmacist if you are not sure a medicine is right for you or your child.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

Quick answers

What is Avagard?
Avagard is a brand name of Alcohol and chlorhexidine gluconate, an over-the-counter medicine. The FDA NDC Directory lists 1 Avagard product in 1 strength and form.
Who makes Avagard?
Solventum holds the FDA application for Avagard (NDA021074, approved June 7, 2001).
Is there a generic or store brand of Avagard?
Other products of Alcohol and chlorhexidine gluconate are listed with the FDA, but none in exactly the same strength and form as a Avagard product.
Has Avagard been recalled?
No recall linked to Avagard products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Avagard is

Each Avagard product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.

Alcohol and chlorhexidine gluconate · over-the-counter medicine

Strength and formProduct namesSame medicine, other namesLabel
alcohol 506.3 mg/mL · chlorhexidine gluconate 8.3 mg/mL
lotion (topical)
3M Avagard None listed DailyMed

Its page quotes the Drug Facts label and lists every brand and store brand: Alcohol and chlorhexidine gluconate →

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Avagard products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA021074SolventumJune 7, 20011

Companies that list Avagard

The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Avagard products.

Recalls

No recall linked to Avagard products (by their NDC code or label) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026

Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.

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