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#
Contacts and useful links#
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
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0220-9235-41 | MotionCalm | 80 in 1 TUBE | PELLET | 80 | 1 | |
| 0220-9235-42 | MotionCalm | 2 in 1 BOX | PELLET | 2 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- MotionCalm
- ANAMIRTA COCCULUS SEED, IPECAC, STRYCHNOS NUX-VOMICA SEED, TOBACCO LEAF, KEROSENE
- IPECAC
- ANAMIRTA COCCULUS SEED
- SUCROSE
- STRYCHNOS NUX-VOMICA SEED
- TOBACCO LEAF
- LACTOSE, UNSPECIFIED FORM
- KEROSENE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 0220-9235 | 0220-9235-41, 0220-9235-42 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| IPECAC | 62I3C8233L | ACTIB |
| ANAMIRTA COCCULUS SEED | 810258W28U | ACTIB |
| SUCROSE | C151H8M554 | IACT |
| STRYCHNOS NUX-VOMICA SEED | 269XH13919 | ACTIB |
| TOBACCO LEAF | 6YR2608RSU | ACTIB |
| LACTOSE, UNSPECIFIED FORM | J2B2A4N98G | IACT |
| KEROSENE | 1C89KKC04E | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| MotionCalm | ANAMIRTA COCCULUS SEED, IPECAC, STRYCHNOS NUX-VOMICA SEED, TOBACCO LEAF, KEROSENE | Boiron | 1ea4de81-3ec0-e9e4-e063-6294a90a7ac9 | 2024-08-01 | 0220-9235-42 0220-9235-41 0220-9235 00220923542 00220923541 1ea4de81-3ec1-e9e4-e063-6294a90a7ac9 1ea4de81-3ec0-e9e4-e063-6294a90a7ac9 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.

