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Over-the-counter medicine · no prescription needed

Dextromethorphan and pyrilamine

Allergy

Official FDA data, not advice

The label text is quoted exactly as the company filed it with the U.S. Food and Drug Administration (FDA), with a link to the official copy. The list of brands comes from the FDA NDC Directory.

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

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

Quick answers

What is Dextromethorphan and pyrilamine used for?
The Drug Facts label of Capron DM (Capital Pharmaceutical, LLC) lists these uses: temporarily relieves these symptoms due to hay fever (allergic rhinitis) or other upper respiratory allergies: runny nose sneezing itching of the nose or throat itchy, watery eyes cough due to minor throat and bronchial irritation associated with a cold alleviates cough to help you sleep nonnarcotic cough suppressant for the relief of cough.
Do I need a prescription for Dextromethorphan and pyrilamine?
No. The products on this page are sold without a prescription (over the counter).
Is a store brand the same as the name brand?
Products listed together below have the same active ingredients, in the same amount and the same form, as registered with the FDA. Inactive ingredients (such as colors, flavors and fillers) and package sizes can differ. Compare the “Active ingredient” box on both packages, and ask a pharmacist if you are not sure.
Has Dextromethorphan and pyrilamine been recalled?
No recall linked to these products appears in the FDA enforcement reports we use.

Drug Facts label

Every over-the-counter medicine must carry a “Drug Facts” box in the same order, set by FDA rules. Below is the label of one product for each common strength and form, quoted word for word. Your own package can differ (for example, children’s products have other directions): always follow the label on your package.

Capron DM · Capital Pharmaceutical, LLC

Dextromethorphan hydrobromide 7.5 mg/5 mL · Pyrilamine maleate 7.5 mg/5 mL, liquid (oral)

Active ingredient (in each 5 mL teaspoonful)

Dextromethorphan HBr 7.5 mg Active Ingredients (in each 5 mL teaspoonful) Pyrilamine Maleate 7.5 mg

Purpose

Antitussive Purpose Antihistamine

Uses

temporarily relieves these symptoms due to hay fever (allergic rhinitis) or other upper respiratory allergies: runny nose sneezing itching of the nose or throat itchy, watery eyes cough due to minor throat and bronchial irritation associated with a cold alleviates cough to help you sleep nonnarcotic cough suppressant for the relief of cough

Warnings

Do not exceed recommended dosage. a persistent cough may be a sign of a serious condition. If cough persist for more than 1 week, tends to recur, or is accompanied by a fever, rash, or persistent headache, consult a doctor.

Do not use

this product if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product for persistent or chronic cough such as occurs with smoking, asthma, or emphysema, or if cough is accompanied by excessive phlegm (mucus) unless directed by a doctor

Ask a doctor before use if

you have a breathing problem such as emphysema or chronic bronchitis glaucoma difficulty in urination due to enlargement of the prostate gland

Ask a doctor before use if

you are taking sedatives or tranquilizers .

When using this product

excitability may occur, especially in children may cause marked drowsiness sedatives and tranquilizers may increase drowsiness effect avoid alcoholic beverages use caution when driving a motor vehicle or operating machinery

If pregnant or breast-feeding

ask a health professional before use.

Keep out of reach of children

In case of accidental overdose, seek professional help or contact a Poison Control Center immediately.

Directions

Do not exceed recommended dosage.

Adults and children 12 years of age and over:4 teaspoonfuls every 6-8 hours, not to exceed 16 teaspoonfuls in 24 hours, or as directed by a doctor
Children 6 to under 12 years of age:2 teaspoonfuls every 6-8 hours, not to exceed 8 teaspoonfuls in 24 hours, or as directed by a doctor
Children 2 to under 6 years of age (For Professional Use Only) 1 teaspoonful every 6-8 hours, not to exceed 4 teaspoonfuls in 24 hours, or as directed by a doctor
Children under 2 years of age:Consult a doctor

Inactive ingredients

Citric Acid, Flavor, Magnasweet, Methyl Paraben, Potassium Citrate, Potassium Sorbate, Propyl Paraben, Propylene Glycol, Purified Water, Sorbitol, Sucralose

Questions?

Call 614.638.4622

— FDA label of Capron DM, Capital Pharmaceutical, LLC, effective June 18, 2025. See the official label on DailyMed →

Capron Max · Capital Pharmaceutical, LLC

Dextromethorphan hydrobromide 15 mg/5 mL · Pyrilamine maleate 15 mg/5 mL, liquid (oral)

Active ingredient (in each 5 mL teaspoonful)

Dextromethorphan HBr 15 mg Pyrilamine Maleate 15 mg

Purpose

Dextromethorphan HBr 15 mg ............................ Antitussive Pyrilamine Maleate 15 mg .............................. Antihistamine

Uses

temporarily relieves these symptoms due to hay fever (allergic rhinitis) or other upper respiratory allergies: runny nose sneezing itching of the nose or throat itchy, watery eyes cough due to minor throat and bronchial irritation associated with a cold alleviates cough to help you sleep nonnarcotic cough suppressant for the relief of cough

Warnings

Do not exceed recommended dosage. a persistent cough may be a sign of a serious condition. If cough persist for more than 1 week, tends to recur, or is accompanied by a fever, rash, or persistent headache, consult a doctor.

Do not use

this product if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product for persistent or chronic cough such as occurs with smoking, asthma, or emphysema, or if cough is accompanied by excessive phlegm (mucus) unless directed by a doctor

Ask a doctor before use if

you have a breathing problem such as emphysema or chronic bronchitis glaucoma difficulty in urination due to enlargement of the prostate gland

Ask a doctor before use if

you are taking sedatives or tranquilizers .

When using this product

excitability may occur, especially in children may cause marked drowsiness sedatives and tranquilizers may increase drowsiness effect avoid alcoholic beverages use caution when driving a motor vehicle or operating machinery

If pregnant or breast-feeding

ask a health professional before use.

Keep out of reach of children

In case of accidental overdose, seek professional help or contact a Poison Control Center immediately.

Directions

Do not exceed recommended dosage.

Adults and children 12 years of age and over:2 teaspoonfuls every 6-8 hours, not to exceed 8 teaspoonfuls in 24 hours, or as directed by a doctor
Children 6 to under 12 years of age:1 teaspoonfuls every 6-8 hours, not to exceed 4 teaspoonfuls in 24 hours, or as directed by a doctor
Children under 6 years of ageConsult a doctor

Inactive ingredients

Citric acid, flavor, methylparaben, monoammonium glycrrhizinate, potassium citrate, potassium sorbate, propylene glycol, propylparaben, purified water, sorbitol,sucralose

Questions?

Call 614.638.4622

— FDA label of Capron Max, Capital Pharmaceutical, LLC, effective June 11, 2025. See the official label on DailyMed →

Broncochem Maximum Cough Night · Laboratorio Magnachem International Srl

Dextromethorphan hydrobromide 30 mg/5 mL · Pyrilamine maleate 50 mg/5 mL, syrup (oral)

Active ingredient

OTC - Active Ingredient Section Dextromethorphan HBr Mepyramine maleate

Purpose

OTC-PURPOSE SECTION Antitussive Antihistamine

Uses

Temporarily relieves these symptoms in all formsof acute, subacute, and cronical cough of any origin, it is very effective in colds, rhinitis, pharyngitis, laryngitis, dry cough, smokers cough, ashma, nervous cough.

Warnings

The following side effects may occur, nausea, vomiting, dizziness, headache, or nervousness may occur, if any of these effects last or worsen, contact your doctor or pharmacist immediately. Stop using this medicine and tell your doctor right away if you have dizziness, nervousness, or trouble sleeping. Do Not Use Stop using this medicine and contact your doctor right away if any of these unlikely but serious side effects occur, fast and irregular heartbeat, mental mood changes such as confusion, hallucinations, nervousness, seizures, tremor, problems with to pee. If you are taking any monoamine oxidase inhibitor (MAOI), or two weeks after stopping them (certain medications for depression or psycological conditions may contain them). If you are not sure if your prescription contains an MAOI, coinsult a professional of health before taking this product. Ask a doctor/pharmacist

Ask a doctor before use if

yoy have Liver disease, heart disease, high blood pressure, thyroid disease, diabetes, trouble urinating due to enlarged prostate gland, cough that occurs with too much phlegm (mucus), presistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema.

Stop use and ask a doctor if

Symptoms last more than 7 days, symptoms worsen or come back, you develop a headache that wont go away, fever, or skin rash.

If pregnant or breast-feeding

ask a health professional before use. Keep Out of the Reach of Children In case of accidental overdose, seek professional help or go to poison control center immediately.

Directions

Do not exceed 4 doses in a 24 hour period. Adult and children 12 years and older: 10 mL 3-4 times a day. Children 6 to under 12 years old: 5 mL 3-4 times a day.

Inactive ingredients

Sugar, Sodium Benzoate, FD&C Yellow #5, Orange flavor, MEthyl paraben, Propyl paraben, ethyl alcohol 95%, Sorbitol 70%, Purified water.

— FDA label of Broncochem Maximum Cough Night, Laboratorio Magnachem International Srl, effective March 23, 2025. See the official label on DailyMed →

Broncochem Maximum Cough Night · Laboratorio Magnachem International Srl

Dextromethorphan hydrobromide 15 mg/5 mL · Pyrilamine maleate 6 mg/5 mL, syrup (oral)

Active ingredient

OTC - Active Ingredient Section Dextromethorphan HBr Mepyramine maleate

Purpose

OTC-PURPOSE SECTION Antitussive Antihistamine

Uses

Temporarily relieves these symptoms in all formsof acute, subacute, and cronical cough of any origin, it is very effective in colds, rhinitis, pharyngitis, laryngitis, dry cough, smokers cough, ashma, nervous cough.

Warnings

The following side effects may occur, nausea, vomiting, dizziness, headache, or nervousness may occur, if any of these effects last or worsen, contact your doctor or pharmacist immediately. Stop using this medicine and tell your doctor right away if you have dizziness, nervousness, or trouble sleeping. Do Not Use Stop using this medicine and contact your doctor right away if any of these unlikely but serious side effects occur, fast and irregular heartbeat, mental mood changes such as confusion, hallucinations, nervousness, seizures, tremor, problems with to pee. If you are taking any monoamine oxidase inhibitor (MAOI), or two weeks after stopping them (certain medications for depression or psycological conditions may contain them). If you are not sure if your prescription contains an MAOI, coinsult a professional of health before taking this product. Ask a doctor/pharmacist

Ask a doctor before use if

yoy have Liver disease, heart disease, high blood pressure, thyroid disease, diabetes, trouble urinating due to enlarged prostate gland, cough that occurs with too much phlegm (mucus), presistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema.

Stop use and ask a doctor if

Symptoms last more than 7 days, symptoms worsen or come back, you develop a headache that wont go away, fever, or skin rash.

If pregnant or breast-feeding

ask a health professional before use. Keep Out of the Reach of Children In case of accidental overdose, seek professional help or go to poison control center immediately.

Directions

Do not exceed 4 doses in a 24 hour period. Adult and children 12 years and older: (5 or 10 mL) 3 times a day. Children between 6 to 12 years old: (2.5 mL) 3 times a day.

Inactive ingredients

Sugar, Sodium Benzoate, FD&C Yellow #5, Orange flavor, MEthyl paraben, Propyl paraben, ethyl alcohol 95%, Sorbitol 70%, Purified water.

— FDA label of Broncochem Maximum Cough Night, Laboratorio Magnachem International Srl, effective April 22, 2024. See the official label on DailyMed →

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

Same medicine, other brands

Each group lists the products that have exactly the same active ingredients, in the same amount and form, as registered with the FDA (NDC Directory). A store brand in the same group has the same medicine as the name brand; inactive ingredients, flavors and package sizes can differ. Each product links to its own official label.

Dextromethorphan hydrobromide 7.5 mg/5 mL · Pyrilamine maleate 7.5 mg/5 mL · liquid (oral) · 2 products

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Capron DM Capital Pharmaceutical, LLC DailyMed
Pyrilamine Maleate and Dextromethorphan Hydrobromide Westminster Pharmaceuticals, LLC DailyMed
Dextromethorphan hydrobromide 15 mg/5 mL · Pyrilamine maleate 15 mg/5 mL · liquid (oral) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Capron Max Capital Pharmaceutical, LLC DailyMed
Dextromethorphan hydrobromide 30 mg/5 mL · Pyrilamine maleate 50 mg/5 mL · syrup (oral) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Broncochem Maximum Cough Night Laboratorio Magnachem International Srl DailyMed
Dextromethorphan hydrobromide 15 mg/5 mL · Pyrilamine maleate 6 mg/5 mL · syrup (oral) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Broncochem Maximum Cough Night Laboratorio Magnachem International Srl DailyMed

What pharmacies pay (NADAC)

The National Average Drug Acquisition Cost (NADAC) is the average price U.S. retail pharmacies paid to buy one unit of a medicine (one tablet, one mL or one gram), from a monthly survey of pharmacy invoices by the Centers for Medicare & Medicaid Services (CMS). State Medicaid programs use it to pay pharmacies.

This is not the price you pay. What you pay depends on your insurance (copay or coinsurance), your pharmacy and any discounts, and pharmacies also charge for filling a prescription. Ask your pharmacist or your health plan what your price will be.

NADAC per unit for Dextromethorphan and pyrilamine, by strength and form
Strength and formGeneric or brandPharmacies pay
dextromethorphan hydrobromide 7.5 mg/5 mL · pyrilamine maleate 7.5 mg/5 mL
liquid
Brand: Capron DM $0.0696 per mL

NADAC list of November 4, 2026; these prices took effect on October 21, 2026. Shown only where a package’s NDC code matches the NADAC list exactly, and only for that exact strength and form: nothing is averaged across strengths. Strengths and forms not listed here have no NADAC price.

Source: NADAC (National Average Drug Acquisition Cost) 2026, data.medicaid.gov (CMS) →

Companies that sell this medicine

The company named on the package (maker or distributor), as listed in the FDA NDC Directory, with its number of over-the-counter products of this medicine.

Recalls

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

Sources

  1. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  4. FDA rule for the Drug Facts label (21 CFR 201.66)

Only medicines marketed under FDA rules for nonprescription drugs (an FDA monograph or an FDA approval) are listed. Homeopathic products are not listed: the FDA does not evaluate them for safety or effectiveness.

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