FDA.reportPublic FDA data

Jet-Avert Motion Sickness Aid

Manufacturer
Bell Pharmaceuticals, Inc.
Effective date
2023-12-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:18:14

Label at a glance#

ProductJet-Avert Motion Sickness Aid
Active ingredientMECLIZINE HYDROCHLORIDE
Label structure8 sections

Indications and uses

prevent and treats nausea, vomiting, or dizziness associated with motion sickness

Dosage and administration

take first dose one hour before starting activity  adults and children 12 years and over  take 1 to 2 tablets once daily, or as directed by a doctor  children under 12 years  do not ues unless directed by doctor

Label contents#

Full prescribing information#

Active ingredient (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Meclizine HCL 25mg

Purpose

OTC - PURPOSE SECTION

Antiemetic

Uses

INDICATIONS & USAGE SECTION

  • prevent and treats nausea, vomiting, or dizziness associated with motion sickness

Warnings

WARNINGS SECTION

Do not use

OTC - DO NOT USE SECTION

  • for children under 12 years of age unless directed by a doctor

Ask a doctor  before use if you have

OTC - ASK DOCTOR SECTION

  • a breathing problem such as emphysema or chronic bronchitis
  • glaucome 
  • difficulty in urination due to enlargement prostate glad

Ask a doctor or pharmacist before useif you are taking

OTC - ASK DOCTOR/PHARMACIST SECTION

  • Sedatives • tranquilizers

When using this product

OTC - WHEN USING SECTION

• drowsiness may occur • alcohol, sedatives, and tranquilizers may increase drowsiness • avoid alcoholic drinks • be careful when driving or operating machinery

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • take first dose one hour before starting activity
 adults and children 12 years and over take 1 to 2 tablets once daily, or as directed by a doctor
 children under 12 years do not ues unless directed by doctor

Other information

SPL UNCLASSIFIED SECTION

  • store at room temperature between 59°-86°F (15°-30°C)
  • protect from excessive moisture 
  • don not use if tamper-evident seal is broken or missing

Inactive ingredients

INACTIVE INGREDIENT SECTION

calcium stearate, FD&C red#40 aluminum lake, lactose, microcrystalline cellulose, silicon dioxide, sodium starch glycolate

Questions or comments?

OTC - QUESTIONS SECTION

1-800-328-5890 Weekdays 8:30-5:00 CST

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
15579-83715579-837-23

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
CALCIUM STEARATE776XM7047LIACT
FD&C RED NO. 40WZB9127XOAIACT
LACTOSEJ2B2A4N98GIACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
MECLIZINE HYDROCHLORIDEHDP7W44CIOACTIB

Source Document#

Source XML · Source PDF

openFDA label cross-check#

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2ea8fd13-d4ad-343b-e063-6294a90a080b1fe1f806-cbf3-4308-8d70-201756e96cd12025-02-21WarningsExact identifier
spl set id: 1fe1f806-cbf3-4308-8d70-201756e96cd1

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.