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
Meclizine HCl USP 25 mg
Antiemetic
Do not use in children under 12 years of age unless directed by a doctor
Ask a doctor or pharmacist before use it you are taking sedatives or tranquilizers.
If pregnant or breast-feeding, ask a health professional before use.
In case of overdose, get medical help or contact the poison control center immediately.
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
aspartame,croscarmellose sodium, dextrose, FD and C Red #40 Lake, magnesium stearate, maltodextrin, microcrystalline cellulose, natural and artificial flavors, silicon dioxide, sodium sulfate, sugar, tricalcium phosphate.
1-800-645-2158
TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0536-1018-01 | EA - Each | 0536-1018 | 38974734-0ca3-472f-a497-87a548eaec94 | 1 | 2014-09-03 |
| 0536-1018-10 | EA - Each | 0536-1018 | f375fa7f-4c57-4dd0-8d08-870621e0e1e7 | 1 | 2014-10-03 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 63187-306 | 63187-306-10, 63187-306-15, 63187-306-20, 63187-306-30 |
| 0536-1018 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MECLIZINE HYDROCHLORIDE | HDP7W44CIO | ACTIB |
| ASPARTAME | Z0H242BBR1 | IACT |
| CROSCARMELLOSE SODIUM | M28OL1HH48 | IACT |
| DEXTROSE, UNSPECIFIED FORM | IY9XDZ35W2 | IACT |
| FD&C RED NO. 40 | WZB9127XOA | IACT |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| MALTODEXTRIN | 7CVR7L4A2D | IACT |
| MICROCRYSTALLINE CELLULOSE | OP1R32D61U | IACT |
| SILICON DIOXIDE | ETJ7Z6XBU4 | IACT |
| SODIUM SULFATE | 0YPR65R21J | IACT |
| SUCROSE | C151H8M554 | IACT |
| TRICALCIUM PHOSPHATE | K4C08XP666 | IACT |
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 |
|---|---|---|---|---|---|---|
| 8b80d3d4-a985-438d-90d0-f896b8c13906 | 5c1a89de-6191-4012-8bc2-8bfc42b89cbd | 2024-10-01 | Warnings | 5c1a89de-6191-4012-8bc2-8bfc42b89cbd |
Adverse event summaries are temporarily unavailable. Other product information remains available.