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Brand-name over-the-counter medicine

Mucosan

Generic names: Dextromethorphan, guaifenesin and phenylephrine · Acetaminophen, dextromethorphan, guaifenesin and phenylephrine

Company: Menper Distributors, Inc.

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 Mucosan?
Mucosan is a brand name of Dextromethorphan, guaifenesin and phenylephrine and Acetaminophen, dextromethorphan, guaifenesin and phenylephrine, an over-the-counter medicine. The FDA NDC Directory lists 5 Mucosan products in 4 strengths and forms.
Who makes Mucosan?
Menper Distributors, Inc. lists 5 of the 5 Mucosan products in the FDA NDC Directory.
Is there a generic or store brand of Mucosan?
Yes. The FDA NDC Directory lists 64 other products with the same active ingredients, strength and form as a Mucosan product, 64 of them generic or store brands. Ask your pharmacist whether one is right for you.
Has Mucosan been recalled?
No recall linked to Mucosan products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Mucosan is

Each Mucosan 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.

Dextromethorphan, guaifenesin and phenylephrine · over-the-counter medicine

Strength and formProduct namesSame medicine, other namesLabel
dextromethorphan hydrobromide 10 mg/5 mL · guaifenesin 100 mg/5 mL · phenylephrine hydrochloride 5 mg/5 mL
liquid (oral)
Mucosan Multi-Symptom Honey, Mucosan Multi-Symptom Cherry 8 products, 7 companies DailyMed
dextromethorphan hydrobromide 20 mg/20 mL · guaifenesin 400 mg/20 mL · phenylephrine hydrochloride 10 mg/20 mL
liquid (oral)
Mucosan Severe Multi-Symptom 29 products, 25 companies DailyMed
dextromethorphan hydrobromide 5 mg/5 mL · guaifenesin 50 mg/5 mL · phenylephrine hydrochloride 2.5 mg/5 mL
liquid (oral)
Mucosan Childrens Multi-Symptom Grape 2 products, 2 companies DailyMed

Its page quotes the Drug Facts label and lists every brand and store brand: Dextromethorphan, guaifenesin and phenylephrine →

Acetaminophen, dextromethorphan, guaifenesin and phenylephrine · over-the-counter medicine

Strength and formProduct namesSame medicine, other namesLabel
acetaminophen 650 mg/20 mL · dextromethorphan hydrobromide 20 mg/20 mL · guaifenesin 400 mg/20 mL · phenylephrine hydrochloride 10 mg/20 mL
liquid (oral)
Mucosan Max with Acetaminophen 25 products, 20 companies DailyMed

Its page quotes the Drug Facts label and lists every brand and store brand: Acetaminophen, dextromethorphan, guaifenesin and phenylephrine →

FDA approval

Mucosan products are sold under an FDA over-the-counter monograph: rules that set the allowed active ingredients, strengths and label wording, so these products do not need an individual FDA approval.

Companies that list Mucosan

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

  • Menper Distributors, Inc.5 products

Recalls

No recall linked to Mucosan 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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