MotionCalm

Manufacturer
Boiron | Boiron, Inc.
Effective date
2024-08-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:27:42

Label at a glance#

ProductMotionCalm
Active ingredientIPECAC, ANAMIRTA COCCULUS SEED, STRYCHNOS NUX-VOMICA SEED, TOBACCO LEAF, KEROSENE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients**

Cocculus indicus 4C HPUS (0.9 mg) (contains less than 10-10 mg picrotoxinin)

Ipecacuanha 4C HPUS (0.9 mg) (contains less than 10-10 mg emetine alkaloids)

Nux vomica 4C HPUS (0.9 mg) (contains less than 10-10 mg strychnine alkaloids)

Petroleum 4C HPUS (0.9 mg) (contains less than 10-11 mg aromatic hydrocarbons)

Tabacum 4C HPUS (0.9 mg) (contains less than 10-10 mg nicotine alkaloids)

The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

OTC - PURPOSE SECTION

Purpose*

Prevents & Relieves Motion Sickness Symptoms: Nausea, Vomiting, Dizziness

INDICATIONS & USAGE SECTION

Uses*

for prevention and treatment of nausea, vomiting, or dizziness associated with motion sickness due to:

  • travel
  • amusement rides
  • video games

OTC - STOP USE SECTION

Stop use and ask a doctor if symptoms persist for more than 2 days or worsen.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental overdose, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 2 years of age and older: For prevention, dissolve 5 pellets under the tongue before activity. For treatment, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved.
  • Children under 2 years of age: Ask a doctor.

INACTIVE INGREDIENT SECTION

lactose, sucrose

OTC - QUESTIONS SECTION

1-800-264-7661

Distributed by Boiron, Inc.

Newtown Square, PA

19073

SPL UNCLASSIFIED SECTION

  • do not use if glued carton end flaps are open or if pellet dispenser seal is broken
  • contains 0.25g of sugar per dose

2 PORTABLE TUBES

APPROX. 80 PELLETS EACH

TOTAL 160 PELLETS

PREVENTS & RELIEVES

MOTION SICKNESS*

*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
**C,K,CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabellabellabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-9235-41MotionCalm80 in 1 TUBEPELLET801
0220-9235-42MotionCalm2 in 1 BOXPELLET21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-9235MOTIONCALM (ANAMIRTA COCCULUS SEED, IPECAC, STRYCHNOS NUX-VOMICA SEED, TOBACCO LEAF, KEROSENE) PELLET [BOIRON]1Current NDC, 2 package rows20240802_1ea4de81-3ec0-e9e4-e063-6294a90a7ac9.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0220-92350220-9235-41, 0220-9235-42

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
MotionCalmANAMIRTA COCCULUS SEED, IPECAC, STRYCHNOS NUX-VOMICA SEED, TOBACCO LEAF, KEROSENEBoiron1ea4de81-3ec0-e9e4-e063-6294a90a7ac92024-08-01Exact identifier
ndc (package): 0220-9235-42
ndc (package): 0220-9235-41
ndc (product): 0220-9235
ndc11 (package): 00220923542
ndc11 (package): 00220923541
spl id: 1ea4de81-3ec1-e9e4-e063-6294a90a7ac9
spl set id: 1ea4de81-3ec0-e9e4-e063-6294a90a7ac9

Reported adverse events (FAERS/openFDA)#

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