Indications and uses
prevents and treats nausea, vomiting or dizziness due to motion sickness
prevents and treats nausea, vomiting or dizziness due to motion sickness
Dosage should be taken one hour before travel starts. Adults and children 12 years of age and older: Chew 1-2 tablets once daily or as directed by a doctor Children under 12 years: do not give this product to children under 12 years of age unless directed by a doctor.
store at room temperature
Meclizine HCl, USP 25 mg
Antiemetic
prevents and treats nausea, vomiting or dizziness due to motion sickness
Do not use in children under 12 years of age unless directed by a doctor.
Ask a doctor before use if you have
Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers.
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 the poison control center immediately.
aspartame, croscarmellose sodium, dextrose, FD&C Red #40 Lake, magnesium stearate, maltodextrin, microcrystalline cellulose, natural and artificial flavors, silicon dioxide, sodium sulfate, sugar, tricalcium phosphate.
If you have any questions or comments or to report an adverse event, please contact (800) 795-9775.
Distributed by: Plus Pharma, Commack, NY 11725
*Plus Pharma is not affiliated with the owner of the registered trademark Bonine®.
When using this product
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51645-994-01 | EA - Each | 51645-994 | 094ec1d6-7d2f-47b2-bfba-42e4d43dd5be | 1 | 2016-03-04 |
| 51645-994-10 | EA - Each | 51645-994 | 1e7b29ee-6984-4e20-aacf-83d5b646caee | 1 | 2016-03-04 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 68071-2178 | 68071-2178-2, 68071-2178-3, 68071-2178-4, 68071-2178-6 |
| 51645-994 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ASPARTAME | Z0H242BBR1 | IACT |
| SUCROSE | C151H8M554 | IACT |
| CROSCARMELLOSE SODIUM | M28OL1HH48 | IACT |
| DEXTROSE | IY9XDZ35W2 | IACT |
| FD&C RED NO. 40 | WZB9127XOA | IACT |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| MALTODEXTRIN | 7CVR7L4A2D | IACT |
| CELLULOSE, MICROCRYSTALLINE | OP1R32D61U | IACT |
| SILICON DIOXIDE | ETJ7Z6XBU4 | IACT |
| SODIUM SULFATE | 0YPR65R21J | IACT |
| TRICALCIUM PHOSPHATE | K4C08XP666 | IACT |
| MECLIZINE HYDROCHLORIDE | HDP7W44CIO | ACTIB |
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 1d75906d-238a-f76c-e063-6294a90ac963 | 6f9010fe-e033-22cc-e053-2a91aa0a361e | 2024-07-17 | Warnings | 6f9010fe-e033-22cc-e053-2a91aa0a361e |
Adverse event summaries are temporarily unavailable. Other product information remains available.