Kids Travel Sickness

Manufacturer
KEYSUN PTY. LIMITED Also Traded as KEYSUN LABORATORIES
Effective date
2014-05-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:05:42

Label at a glance#

ProductKids Travel Sickness
Active ingredientJATEORHIZA CALUMBA ROOT, STRYCHNOS NUX-VOMICA SEED, SODIUM BORATE
Label structure9 sections

Storage and handling

STORE BELOW 30 C

Label contents#

Full prescribing information#

INACTIVE INGREDIENT SECTION

Non-Active Ingredients

Isomalt, Natural Strawberry Flavour,

Natural Colour Carmine E120 (Cochineal).

OTC - ACTIVE INGREDIENT SECTION

Each Lozenge Contains

Cocculus 30C, Nux Vomica 30C,

Borax 6C in equal quantities

OTC - PURPOSE SECTION

Indications

For natural temporary relief of

motion sickness and nausea

WARNINGS SECTION

Warning: If symptoms persist or worsen suddenly, consult your health-care

specialist.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all other medicine out of the reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions

For best results, begin taking one Kids Travel Sickness

15-20 minutes before travel. The lozenge should be licked

or sucked and does not need to be finished as the

therapeutic benefit will be gained in the first few licks.

If on a long journey, suck another lozenge if needed. Not

to be used in children under 2 years of age without medical advice.

Recommended dosage up to 3 per day.

STORAGE AND HANDLING SECTION

STORE BELOW 30 C

INDICATIONS & USAGE SECTION

Indications

For natural, temporary relief of motion sickness

and nausea

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

copy of labelcopy of label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64997-050-012019-11-27C16284748780-19855e2a2-4230-60a7-e053-dbdaa90a05bdHomeopathic Drug Facts
64997-050-022019-11-27C16284748780-19855e2a2-4230-60a7-e053-dbdaa90a05bdHomeopathic Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64997-050-01Kids Travel Sickness10 in 1 BOXLOZENGE101
64997-050-02Kids Travel Sickness10 in 1 BOXLOZENGE101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64997-050KIDS TRAVEL SICKNESS (COCCULUS 30C, NUX VOMICA 30C, BORAX 6C) LOZENGE [KEYSUN PTY. LIMITED ALSO TRADED AS KEYSUN LABORATORIES]1Legacy NDC, 2 package rows20140502_c05c04fc-bc37-4597-a5f7-2a070e947293.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
JATEORHIZA CALUMBA ROOTACTIVE INGREDIENTV36I2B8LD51
SODIUM BORATEACTIVE INGREDIENT91MBZ8H3QO1
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH139191
BORATE IONACTIVE MOIETY44OAE30D221
JATEORHIZA CALUMBA ROOTACTIVE MOIETYV36I2B8LD51
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH139191
ISOMALTINACTIVE INGREDIENTS870P55O2W1

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64997-05064997-050-01, 64997-050-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 5 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ISOMALTISOMALTS870P55O2WPOWDER / SUBLINGUAL530 mgExact identifier — unii candidate
5 equally ranked IID candidates
ISOMALTISOMALTS870P55O2WTABLET, CHEWABLE / ORAL630 mgExact identifier — unii candidate
5 equally ranked IID candidates
ISOMALTISOMALTS870P55O2WTABLET / ORAL522 mgExact identifier — unii candidate
5 equally ranked IID candidates
ISOMALTISOMALTS870P55O2WCAPSULE / ORAL158 mgExact identifier — unii candidate
5 equally ranked IID candidates
ISOMALTISOMALTS870P55O2WTROCHE / ORAL1718.71 mgExact identifier — unii candidate
5 equally ranked IID candidates

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
69b58ad6-892b-457a-bbb8-9f93e3fd62b4c05c04fc-bc37-4597-a5f7-2a070e9472932014-05-01WarningsExact identifier
spl id: 69b58ad6-892b-457a-bbb8-9f93e3fd62b4
spl set id: c05c04fc-bc37-4597-a5f7-2a070e947293

Reported adverse events (FAERS/openFDA)#

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