Indications and uses
for prevention and treatment of nausea, vomiting, or dizziness associated with motion sickness
for prevention and treatment of nausea, vomiting, or dizziness associated with motion sickness
do not take more than directed dosage should be taken one hour before travel starts chew or crush tablets completely before swallowing; do not swallow tablets whole adults and children 12 years and over: take 1 to 2 chewable tablets once daily or as directed by a doctor
TAMPER EVIDENT: DO NOT USE IF OUTER PACKAGE IS OPENED OR BLISTER IS TORN OR BROKEN store at 25ºC (77ºF); excursions permitted between 15º-30ºC (59º-86ºF) protect from heat and humidity see end flap for expiration date and lot number
Meclizine HCl 25 mg
Antiemetic
for prevention and treatment of nausea, vomiting, or dizziness associated with motion sickness
for children under 12 years of age unless directed by a doctor.
taking sedatives or tranquilizers.
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away.
colloidal silicon dioxide, dextrose, FD&C red #40 aluminum lake, flavor, lactose monohydrate, magnesium stearate, pregelatinized starch, propylene glycol, saccharin sodium, silicon dioxide
1-800-426-9391
NDC 11822-4040-1
Compare to the active ingredient
in Bonine® Chewable Tablets*
MOTION SICKNESS RELIEF
MECLIZINE HCl 25 mg CHEWABLE TABLETS
ANTIEMETIC
PREVENTS MOTION SICKNESS
Ages 12 Years and Over
RASPBERRY
FLAVORED
16 CHEWABLE TABLETS
ACTUAL SIZE
Chew or crush tablets completely
before swallowing.
TAMPER EVIDENT: DO NOT USE IF PACKAGE
IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN
OR SHOWS ANY SIGNS OF TAMPERING
*This product is not manufactured or distributed by
WellSpring Pharmaceutical Corporation, owner of the
registered trademark Bonine® Chewable Tablets.
50844 ORG082340421
DISTRIBUTED BY: RITE AID,
200 NEWBERRY COMMONS
ETTERS, PA 17319
www.riteaid.com
SATISFACTION
GUARANTEE
If you're not satisfied, we'll
happily refund your money.

| Class | Version | Type | Effective |
|---|---|---|---|
| MECLIZINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0011822372787 | GTIN-13: 0011822372787 EAN-13: 0011822372787 GTIN-12: 011822372787 UPC-A: 011822372787 GTIN storage (14 digits): 00011822372787 | rite-aid-44-404a-1.jpg |
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| ac6963c4-31c6-325f-ee58-83a0a06597ad | Product name | 5 | 20221206 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 11822-4040-1 | Motion Sickness Relief | 8 in 1 BLISTER PACK | TABLET, CHEWABLE | 8 | 4 | |
| 11822-4040-1 | Motion Sickness Relief | 2 in 1 CARTON | TABLET, CHEWABLE | 2 | 4 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 11822-4040 | 11822-4040-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MECLIZINE HYDROCHLORIDE | 008PUV3986 | ACTIB |
| SILICON DIOXIDE | ETJ7Z6XBU4 | IACT |
| DEXTROSE, UNSPECIFIED FORM | IY9XDZ35W2 | IACT |
| FD&C RED NO. 40 ALUMINUM LAKE | 6T47AS764T | IACT |
| LACTOSE MONOHYDRATE | EWQ57Q8I5X | IACT |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| STARCH, CORN | O8232NY3SJ | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| SACCHARIN SODIUM | SB8ZUX40TY | 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 |
|---|---|---|---|---|---|---|
| Motion Sickness Relief | MECLIZINE HCL | Rite Aid Corporation | e599dc64-ac10-4f4e-9318-e9fab0526488 | 2025-11-15 | Warnings | 11822-4040-1 11822-4040 11822404001 c9a8fed3-0e78-4eaf-b368-a39e8b48841b e599dc64-ac10-4f4e-9318-e9fab0526488 |
Adverse event summaries are temporarily unavailable. Other product information remains available.