FDA.reportPublic FDA data

Genexa Motion Sickness Relief

Manufacturer
Genexa Inc.
Effective date
2023-01-20
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 02:19:46

Label at a glance#

ProductGenexa Motion Sickness Relief
Active ingredientBRYONIA ALBA WHOLE, CINNAMON, ANAMIRTA COCCULUS SEED, COLCHICUM AUTUMNALE BULB, IRIS VERSICOLOR ROOT, POTASSIUM CARBONATE, NUTMEG, DELPHINIUM STAPHISAGRIA SEED, TOBACCO LEAF, GINGER
Label structure13 sections

Storage and handling

Other information store between 20-25° C (68-77° F) in a dry place out of direct sunlight.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Keep outer package for complete product information
Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredients ‡**

Bryonia alba 6X HPUS

Cinnamonum 6X HPUS

Cocculus indica 30X HPUS

Colchicum autumnale (M) 12X

Iris versicolor (N) 12X HPUS

Kali carbonicum 6X HPUS

Nux moschata 6X HPUS

Staphysagria 6X HPUS

Tabacum 30X HPUS

Zingiber officinale 6X HPUS

‡ Organic

"HPUS" indicates that this ingredient is officially included in the Homeopathic Pharmacopoeia of the United States.

OTC - PURPOSE SECTION

Purpose

headache, loss of appetite and vomiting

nausea and vomiting

headache, nausea and vomiting

salivation and dizziness

vomiting and dizziness

loss of appetite

drowsiness and fatigue

headache and fatigue

nausea, vomiting and cold perspiration

loss of appetite and nausea

INDICATIONS & USAGE SECTION

Uses*

addresses the following symptoms associated with motion sickness:

  • nausea
  • vomiting
  • dizziness

WARNINGS SECTION

Warnings

OTC - STOP USE SECTION

Stop use and ask a doctor if symptoms persist for more than 3 days or worsen.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions

adults and children 12 years

of age and older

  • chew 2 tablets at the onset of symptoms
  • do not swallow whole
  • repeat every 4-6 hours as needed
children 3-11 years of age
  • chew 1 tablet at the onset of symptoms
  • do not swallow whole
  • repeat every 4-6 hours as needed
children under 3 years of ageask a doctor before use

STORAGE AND HANDLING SECTION

Other information

store between 20-25° C (68-77° F) in a dry place out of direct sunlight.

INACTIVE INGREDIENT SECTION

Inactive ingredients

organic acai berry flavor, organic carnauba wax, organic dextrose, organic maltodextrin, organic rice bran extract

OTC - QUESTIONS SECTION

Questions?

1-855-436-3921

SPL UNCLASSIFIED SECTION

* CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT EVALUATED BY THE FOOD AND DRUG ADMINISTRATION.

** X is a homeopathic dilution:

see genexa.com for more information.

SPL UNCLASSIFIED SECTION

Bottle is safety sealed with a perforated band around the bottle. DO NOT use if bottle seal is disturbed or missing.

Patent Pending | Distributed by:

Genexa Inc. Atlanta, GA 30318

genexa.com
Certified Organic by SCS Global Services

SPL UNCLASSIFIED SECTION

Made in the USA with globally sourced ingredients

R-20220209

NDC 69676-0028-1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Genexa

Motion Sickness Relief

Organic Motion Sickness Relief Formula*Nausea*

Nausea*

Dizziness*

Vomiting*

Know you ingredients

Made with Organic Acai Berry Flavor

Made without: common allergens, artificial dyes, or parabens

Homeopathic

60 Chewable Tablets

Unit CartonUnit Carton

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69676-0028-12025-01-30C16284748780-12cef2736-9577-d83d-e063-dadaa90ab31fMotion Sickness Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69676-0028-1Genexa Motion Sickness Relief60 in 1 BOTTLE, PLASTICTABLET, CHEWABLE606
69676-0028-1Genexa Motion Sickness Relief1 in 1 CARTONTABLET, CHEWABLE16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69676-0028GENEXA MOTION SICKNESS RELIEF (BRYONIA ALBA, CINNAMONUM, COCCULUS INDICA, COLCHICUM AUTUMNALE, IRIS VERSICOLOR, KALI CARBONICUM, NUX MOSCHATA, STAPHYSAGRIA, TABACUM, ZINGIBER OFFICINALE) TABLET, CHEWABLE [GENEXA INC.]6Legacy NDC, 2 package rows20230121_9bf2a1d6-8a8f-5737-e053-2a95a90a3d99.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69676-002869676-0028-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
BRYONIA ALBA WHOLE56K0VVT47PACTIB
CINNAMON5S29HWU6QBACTIB
ANAMIRTA COCCULUS SEED810258W28UACTIB
COLCHICUM AUTUMNALE BULB993QHL78E6ACTIB
IRIS VERSICOLOR ROOTX43D4L3DQCACTIB
POTASSIUM CARBONATEBQN1B9B9HAACTIB
NUTMEGAEE24M3MQ9ACTIB
DELPHINIUM STAPHISAGRIA SEED00543AP1JVACTIB
TOBACCO LEAF6YR2608RSUACTIB
MALTODEXTRIN7CVR7L4A2DIACT
RICE BRANR60QEP13ICIACT
DEXTROSEIY9XDZ35W2IACT
GINGERC5529G5JPQACTIB
CARNAUBA WAXR12CBM0EIZIACT

Source Document#

Source XML

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
f2b47931-684b-6863-e053-2a95a90ae1529bf2a1d6-8a8f-5737-e053-2a95a90a3d992023-01-20WarningsExact identifier
spl id: f2b47931-684b-6863-e053-2a95a90ae152
spl set id: 9bf2a1d6-8a8f-5737-e053-2a95a90a3d99

Reported adverse events (FAERS/openFDA)#

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