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Brand-name over-the-counter medicine

Hibiclens

Generic name: Chlorhexidine

FDA application holder: Molnlycke Hlth

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 Hibiclens?
Hibiclens is a brand name of Chlorhexidine, an over-the-counter medicine. The FDA NDC Directory lists 2 Hibiclens products in 1 strength and form.
Who makes Hibiclens?
Molnlycke Hlth holds the FDA application for Hibiclens (NDA017768, approved September 17, 1976). 1 other company (repackagers or distributors) also list Hibiclens products.
Is there a generic or store brand of Hibiclens?
Yes. The FDA NDC Directory lists 8 other products with the same active ingredients, strength and form as a Hibiclens product. Ask your pharmacist whether one is right for you.
Has Hibiclens been recalled?
No recall linked to Hibiclens products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Hibiclens is

Each Hibiclens 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.

Chlorhexidine · over-the-counter medicine

Strength and formProduct namesSame medicine, other namesLabel
chlorhexidine gluconate 4%
solution (topical)
Hibiclens 8 products, 6 companies DailyMed

Its page quotes the Drug Facts label and lists every brand and store brand: Chlorhexidine →

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Hibiclens products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA017768Molnlycke HlthSeptember 17, 19762

Companies that list Hibiclens

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

Recalls

No recall linked to Hibiclens 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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