Motion Sickness
Motion Sickness is an FDA drug label for the active ingredient MECLIZINE HCL manufactured by H E B administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260821.
- Generic name
- MECLIZINE HCL
- Manufacturer
- H E B
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 37808-903
- Application
- M009
- Label effective
- 20260821
About this product
Motion Sickness is an FDA-registered drug product whose active ingredient is MECLIZINE HCL. It is labelled by H E B taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 37808-903, application M009, label effective 20260821. It is one of 18 FDA drug label records sharing the active ingredient MECLIZINE HCL. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing MECLIZINE HCL are most often described in connection with: treatment nausea, vomiting dizziness, motion sickness. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses for the prevention and treatment of nausea, vomiting, or dizziness associated with motion sickness
Dosage & Administration
Directions do not take more than directed take first dose 1/2 to 1 hour before starting activity adults and children 12 years and over: 1 to 2 tablets once daily, or as 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 difficulty in urination due to enlargement of the prostate gland glaucoma a breathing problem such as emphysema or chronic bronchitis Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers. When using this product drowsiness may occur avoid alcoholic beverages alcohol, sedatives, and tranquilizers may increase drowsiness 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.
More products with the same ingredient
MECLIZINE HCLLess Drowsy Formula Motion Sickness Relief
View labelLess Drowsy Motion Sickness Relief
View labelMeclizine HCL 25 mg
View labelMotion Sickness Relief
View labelHow products containing MECLIZINE HCL compare
FDA lists 18 drug label records with MECLIZINE HCL as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Strategic Sourcing Services LLC | 2 |
| — | — | ARMY AND AIR FORCE EXCHANGE SERVICE | 1 |
| — | — | CVS PHARMACY, INC. | 1 |
| — | — | Cardinal Health 110, LLC. DBA Leader | 1 |
| — | — | DOLGENCORP, LLC | 1 |
Recall and safety notices
5 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.
| Recall | Product | Firm | Class | Status | Reported |
|---|---|---|---|---|---|
| D-0098-2026 | Taoscare Motion Sickness Patches 36-count box, Henan Xinyongtal Medical Technology., Ltd., Address: he nan sheng zhou kou shi huai yang xian gong ye yuan qu, X003SR097N | ibspot | Class II | Ongoing | 20251029 |
| D-1395-2022 | QP MOTION SICKNESS TABLET 8 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022. | Family Dollar Stores, Llc. | Class II | Ongoing | 20220831 |
| D-0325-2020 | Motion Sickness Strips (meclizine hydrochloride) 25 mg strips, 8-count box, Distributed by Sato Pharmaceutical INC. 20695 S. Western Ave., Suite 240 Torrence, CA 90501, NDC 69842-288-01. UPC 5042849946 | Sato Pharmaceutical Inc. | Class III | Terminated | 20191120 |
| D-0323-2020 | Motion Sickness (meclizine hydrochloride) 25 mg tablets, 12-count box, Distributed by Sato Pharmaceutical INC. 20695 S. Western Ave., Suite 240 Torrence, CA 90501, NDC 59779-534-01. UPC 050428345535 | Sato Pharmaceutical Inc. | Class III | Terminated | 20191120 |
| D-0848-2019 | Dr. King's SafeCare Rx Nausea & Motion Sickness, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955005520, NDC 57955-0055-2 | King Bio Inc. | Class I | Terminated | 20190320 |
Frequently asked questions
What is Motion Sickness used for?
Uses for the prevention and treatment of nausea, vomiting, or dizziness associated with motion sickness
Who makes Motion Sickness?
H E B is the labeler of record for Motion Sickness. 18 FDA label records share the active ingredient MECLIZINE HCL, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.
What form does Motion Sickness come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Motion Sickness prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Are there other products containing MECLIZINE HCL?
Yes. 18 FDA drug label records list MECLIZINE HCL as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.
Has Motion Sickness been recalled?
5 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.