Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameMECLIZINE HYDROCHLORIDE
Labeler / manufacturerBryant Ranch Prepack
RouteORAL
Drug classDrug class not supplied in source label
Product NDC71335-2177
Label effective date2026-08-20
Official product label reference
Meclizine Hydrochloride — Bryant Ranch Prepack
This page contains 17 source sections for MECLIZINE HYDROCHLORIDE, oral route. Label set cd82fca9-a8dc-4545-8e64-b67d644832e7, version 104.
Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.
Uses described in the label
Uses prevents and treats nausea, vomiting or dizziness due to motion sickness
Purpose
Purpose Antiemetic
Dosage and administration — label text
Directions Dosage should be taken one hour before travel starts adults and children 12 years of age and over chew 1 to 2 tablets once daily, or as directed by a doctor children under 12 years of age do not give to children under 12 years of age unless directed by a doctor
Table text from source:
| adults and children 12 years of age and over | chew 1 to 2 tablets once daily, or as directed by a doctor
| children under 12 years of age | do not give to children under 12 years of age unless directed by a doctor
Warnings
Warnings Do not use for children under 12 years of age unless directed by a doctor Ask a doctor before use if you have glaucoma a breathing problem such as emphysema or chronic bronchitis trouble urinating due to an enlarged prostate gland Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers When using this product drowsiness may occur alcohol, sedatives, and tranquilizers may increase drowsiness avoid alcoholic drinks 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 (1-800-222-1222).
Active ingredient
Drug Facts Active ingredient (in each chewable tablet) Meclizine HCl 25 mg
Do not use
Do not use for children under 12 years of age unless directed by a doctor
Ask a doctor before use
Ask a doctor before use if you have glaucoma a breathing problem such as emphysema or chronic bronchitis trouble urinating due to an enlarged prostate gland
Ask a doctor or pharmacist
Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers
While using this medicine
When using this product drowsiness may occur alcohol, sedatives, and tranquilizers may increase drowsiness avoid alcoholic drinks use caution when driving a motor vehicle or operating machinery
Pregnancy or breast feeding
If pregnant or breast-feeding, ask a health professional before use.
Child safety
Keep out of reach of children.
Overdose information
In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
Other safety information
Other information Store in a dry place at 15°-30°C (59°-86°F) keep lid tightly closed
Inactive ingredient
Inactive ingredients croscarmellose sodium, crospovidone, FD&C red #40 lake, french vanilla flavor, lactose, magnesium stearate, raspberry flavor, silica, sodium saccharin, stearic acid.
Questions
Questions or comments? 1-800-231-4670
Unclassified section
TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING *This product is not manufactured or distributed by Wellspring Pharmaceutical Corporation, owner of the registered trademark Bonine®. Distributed by: RUGBY® LABORATORIES Indianapolis, IN 46268 (800) 616-2471 www.major-rugby.com Rev. 11/25 R-29 Re-order No. 371033
Supply and packaging
HOW SUPPLIED Meclizine HCl 25 mg NDC: 71335-2177-1: 30 Tablets in a BOTTLE NDC: 71335-2177-2: 20 Tablets in a BOTTLE NDC: 71335-2177-3: 25 Tablets in a BOTTLE NDC: 71335-2177-4: 40 Tablets in a BOTTLE NDC: 71335-2177-5: 60 Tablets in a BOTTLE NDC: 71335-2177-6: 90 Tablets in a BOTTLE NDC: 71335-2177-7: 8 Tablets in a BOTTLE NDC: 71335-2177-8: 14 Tablets in a BOTTLE NDC: 71335-2177-9: 10 Tablets in a BOTTLE NDC: 71335-2177-0: 120 Tablets in a BOTTLE Repackaged/Relabeled by: Bryant Ranch Prepack Burbank, CA 91504
The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.