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Wal-dram 2 quick-dissolving - Medication Information

Product NDC Code 0363-1407
Drug Name

Wal-dram 2 quick-dissolving

Type Brand
Pharm Class Antiemetic [EPC],
Emesis Suppression [PE]
Active Ingredients
Meclizine hydrochloride 25 mg/1
Route ORAL
Dosage Form TABLET, ORALLY DISINTEGRATING
RxCUI drug identifier 1663815,
1800794
Application Number M009
Labeler Name Walgreen Co.
Packages
Package NDC Code Description
0363-1407-01 2 blister pack in 1 carton (0363-1407-01) / 6 tablet, orally disintegrating in 1 blister pack
0363-1407-02 3 blister pack in 1 carton (0363-1407-02) / 6 tablet, orally disintegrating in 1 blister pack
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient (in each tablet) Meclizine hydrochloride 25mg

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 to prevent motion sickness take it at least one hour before traveling adults and children 12 years of age and over: take 1 to 2 (25 to 50 mg) tablets once daily, or as directed by a physician.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients acesulfame potassium, erythritol, hydroxypropyl cellulose, colloidal silicon dioxide, mannitol, menthol, sodium stearyl fumarate, yellow ferric oxide.

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

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Wal-Dram 2 Quick-Dissolving meclizine hydrochloride ERYTHRITOL MANNITOL ACESULFAME POTASSIUM HYDROXYPROPYL CELLULOSE (1600000 WAMW) FERRIC OXIDE YELLOW SODIUM STEARYL FUMARATE SILICON DIOXIDE LEVOMENTHOL MECLIZINE HYDROCHLORIDE MECLIZINE SJ

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.
Carton Image -01 Carton Image -01

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
Ask a doctor before use if you have ■ glaucoma ■ a breathing problem such as emphysema or chronic bronchitis ■ difficulty in urination due to enlargement of the prostate gland

Ask doctor or pharmacist

Information about when a doctor or pharmacist should be consulted about drug/drug or drug/food interactions before using a drug product.
Ask a physician or pharmacist before use if you are ■ taking sedatives or tranquilizers

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use in children under 12 years of age unless directed by a physician

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.

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other information ■ store at 20-30°C (68-86°F)

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 ■ you may get drowsy ■ avoid alcoholic beverages ■ be careful when driving a motor vehicle or operating machinery ■ alcohol, sedatives, and tranquilizers may increase the drowsiness effect

Pregnancy or breast feeding

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

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 physician Ask a doctor before use if you have ■ glaucoma ■ a breathing problem such as emphysema or chronic bronchitis ■ difficulty in urination due to enlargement of the prostate gland Ask a physician or pharmacist before use if you are ■ taking sedatives or tranquilizers When using this product ■ you may get drowsy ■ avoid alcoholic beverages ■ be careful when driving a motor vehicle or operating machinery ■ alcohol, sedatives, and tranquilizers may increase the drowsiness effect 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.

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