Active Ingredient (In Each Tablet)
Meclizine HCl 25mg
The following Structured Product Label (SPL) was submitted to the FDA by Sda Laboratories, Inc. for the product Meclizine (NDC 66424-387). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient (in each tablet), purpose, uses, warnings, when using this product, if pregnant or breast-feeding,, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Meclizine HCl 25mg
Antiemetic
prevents and treats nausea, vomiting or dizziness associated with motion sickness
Do not use for children under 12 years of age unless directed by a doctor.
Do not take unless directed by a doctor if you have
Do not take if you are taking sedatives or tranquilizers, without first consulting your doctor.
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away.
| Adults and children 12 years and over | take 1 or 2 tablets once daily or as directed by doctor |
Croscarmellose sodium, dextrose, FD&C Red#40, flavor, magnesium stearate, microcrystalline cellulose, silicon dioxide, sodium saccharine, stearic acid
Adverse drug event call (800) 687-0176 (M - F, 8AM - 4PM EST).
NDC 66424-0387-01
*Compare to the active ingredient in Bonine®
MECLIZINE
CHEWABLE
Raspberry Flavor
Meclizine HCl 25mg
Anti-Emetic
• Motion Sickness • Nausea • Vomiting
100 TABLETS
SDA
LABORATORIES
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