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Meclizine hcl - Medication Information

Product NDC Code 57237-333
Drug Name

Meclizine hcl

Type Brand
Pharm Class Antiemetic [EPC],
Emesis Suppression [PE]
Active Ingredients
Meclizine hydrochloride 12.5 mg/1
Route ORAL
Dosage Form TABLET
RxCUI drug identifier 995624
Application Number M009.50
Labeler Name Rising Pharma Holdings, Inc.
Packages
Package NDC Code Description
57237-333-01 100 tablet in 1 bottle (57237-333-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Drug Facts Active ingredient (in each tablet) Meclizine HCl, USP 12.5 mg

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions dosage should be taken one hour before travel starts adults and children 12 years and over take 2 or 4 tablets once daily or as directed by a doctor
adults and children 12 years and overtake 2 or 4 tablets once daily or as directed by a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients colloidal silicon dioxide, crospovidone, lactose monohydrate, magnesium stearate, microcrystalline cellulose

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses prevents and treats nausea, vomiting or dizziness associated with motion sickness.

Purpose

Information about the drug product’s indications for use.
Purpose Antiemetic

Spl product data elements

Usually a list of ingredients in a drug product.
Meclizine HCl MECLIZINE HYDROCHLORIDE SILICON DIOXIDE CROSPOVIDONE LACTOSE MONOHYDRATE MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE MECLIZINE HYDROCHLORIDE MECLIZINE White to Off White AB;12

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PRINCIPAL DISPLAY PANEL - 12.5 mg tablets container label NDC 57237-333-01 Meclizine Hydrochloride Tablets, USP 12.5 mg 100 Tablets meclizine-12.5mg-100ct

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or comments? Call 1-844-474-7464 Monday to Friday 8 AM - 5 PM ET Manufactured by: Unique Pharmaceutical Laboratories (A Div. of J.B.Chemicals & Pharmaceuticals Ltd.), Mumbai 400 030, India Mfg. Lic. No.: G/1430 Distributed by: Rising Pharma Holdings, Inc. East Brunswick, NJ 08816 Issued: 02/2024 138528

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product do not exceed recommended dosage may cause drowsiness alcohol, sedatives, and tranquilizers may increase drowsiness avoid alcoholic drinks use caution when driving a motor vehicle or operating machinery

Pregnancy or breast feeding

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

Storage and handling

Information about safe storage and handling of the drug product.
Other information store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature].

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings Do not use in children under 12 years of age unless directed by a doctor. Do not take this product, unless directed by a doctor, if you have glaucoma a breathing problem such as emphysema or chronic bronchitis trouble urinating due to an enlarged prostate gland Do not take this product if you are taking sedatives or tranquilizers, without first consulting your doctor.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API