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Drugs A–Z

Meclizine Hydrochloride

Meclizine Hydrochloride is an over-the-counter medicine. The sections below reproduce one FDA label for it, named under "Label". Products in other forms, strengths or from other makers have their own labels, which can differ.

Type
Over the counter (OTC)
Brand names
Dramamine, Bonine, Dramamine Less Drowsy, Less Drowsy Motion Sickness Relief
Taken
Oral
Label
THE PROCTER & GAMBLE MANUFACTURING COMPANY, revised September 10, 2026 · full label on DailyMed

Purpose

Antiemetic

What it is used for

for the prevention and treatment of nausea, vomiting, or dizziness associated with motion sickness

Active ingredient

Meclizine HCl 25 mg

Do not use

in children under 12 years of age 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 or pharmacist before use if you are

taking sedatives or tranquilizers.

When using this product

drowsiness may occur avoid alcoholic drinks alcohol, sedatives, and tranquilizers may increase drowsiness use caution when driving a motor vehicle or operating machinery

Warnings

Do not use in children under 12 years of age 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 or pharmacist before use if you are taking sedatives or tranquilizers. When using this product drowsiness may occur avoid alcoholic drinks alcohol, sedatives, and tranquilizers may increase drowsiness 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 overdose, get medical help or contact a Poison Control Center right away.

Pregnancy or breastfeeding

If pregnant or breast feeding, ask a health professional before use.

Keep out of reach of children

.

Dosage:
we do not reproduce dosing instructions. The right dose depends on the person and the condition and is set by the prescriber or pharmacist. Dosage section of the full label.

Meclizine in the news

We have not covered this medicine yet. Latest news

Recalls

  • Class II Ongoing

    Meclizine Hydrochloride Tablets, USP 12.5 mg, (a) 50 Tablets [5 x 10] (NDC 60687-775-65) (b) 12.5 mg Individual Dose ( NDC 60687-775-11), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio, 43217.

    Reason: Failed tablet specifications.

    Amerisource Health Services LLC

    Lots, distribution and details
    Lots / codes
    Lot #1024852; Exp 9/30/2026
    Distribution
    U.S. Nationwide
    Quantity
    697 cartons
    Recall started
    March 16, 2026 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0418-2026
  • Class II Ongoing

    Meclizine HCl Tablets, 25 mg, packaged in 100-count HDPE bottle, Distributed by: Rising Pharma Holdings, Inc. East Brunswick, NJ 08816, Manufactured by: Aurex laboratories LLC, East Windsor, NJ 08520, NDC 16571-752-01

    Reason: Labeling: Incorrect Instructions

    RISING PHARMACEUTICALS

    Lots, distribution and details
    Lots / codes
    Lot # CB21024, Exp 2/2023
    Distribution
    to be entered
    Quantity
    1,344 bottles
    Recall started
    September 2, 2021 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0005-2022

Have this medicine at home? Compare the lot number and expiry date on your package with the recall. Do not stop taking a prescribed medicine on your own — stopping suddenly can be riskier than the recalled lot. Your pharmacist can check it and usually swap it for an unaffected one.

Get alerts for Meclizine Hydrochloride

We will email you if the FDA reports a recall, if its shortage status changes, or when we publish news about it — at most one email a day. No account needed.









Source: FDA structured product labeling, retrieved through openFDA. Label text is shown as published by the FDA, without editing; long sections are shortened, marked […]. openFDA data are not validated for clinical use — always check the current label and ask a doctor or pharmacist about your own treatment. Set ID 29a1bd1e-d0e0-478f-e063-6394a90ab0aa.


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Important: this content is for informational purposes only and is not medical advice, a prescribing instruction, or a recommendation to act. Consult a licensed healthcare professional before taking any medication.

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