FDA.reportPublic FDA data

MOTION SICKNESS HP

Manufacturer
Natural Creations, Inc. | OHM Pharma, Inc.
Effective date
2023-01-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:19:40

Label at a glance#

ProductMOTION SICKNESS HP
Active ingredientARNICA MONTANA, BRYONIA ALBA ROOT, QUININE SULFATE, ANAMIRTA COCCULUS SEED, CONIUM MACULATUM FLOWERING TOP, STRYCHNOS IGNATII SEED, IPECAC, POTASSIUM CARBONATE, STRYCHNOS NUX-VOMICA SEED, SEPIA OFFICINALIS JUICE, TOBACCO LEAF, VERATRUM ALBUM ROOT
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS (HPUS*) - equal amounts of: Arnica Montana 30C, Bryonia Alba 30C, Chininum Sulphuricum 30C, Cocculus Indicus 30C, Conium Maculatum 30C, Ignatia Amara 30C, Ipecacuanha 30C, Kali Carbonicum 30C, Nux Vomica 30C, Sepia 30C, Tabacum 30C, Veratrum Album 30C

INDICATIONS & USAGE SECTION

USES: Temporarily relieves symptoms related to motion sickness.**

WARNINGS SECTION

WARNING:

  • Consult a physician for use in children under 12 years of age.
  • IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use.
  • KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.
  • Do not use it TAMPER EVIDENT seal is broken or missing.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: Adults and children above 12 years: 10 drops orally 3 times daily, or as directed by a health care professional.

REFERENCES SECTION

*The letters "HPUS" indicate the components in the product are officially monographed in the Homeopathic Pharmacopeia of the United States.

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Purified Water, USP Ethanol Alcohol 20%

OTC - QUESTIONS SECTION

QUESTIONS AND COMMENTS?

Natural Creations, Inc. / Woodbine, IA 51579 / 712-647-1600

OTC - PURPOSE SECTION

USES: Temporarily relieves symptoms related to motion sickness.**

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 43406-0099-1

MOTION SICKNESS HP

HOMEOPATHIC

1 fl oz (30 mL) / 20% Alcohol

Image Of LabelImage Of Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
22bca8fc-c2b1-897d-b515-117a7522ccaeProduct name320150731

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43406-0099-12023-01-19C16284748780-19855d018-e987-cd31-e053-dbdaa90ab51aMOTION SICKNESS HP
43406-0099-12019-11-27C16284748780-19855d018-e987-cd31-e053-dbdaa90ab51aMOTION SICKNESS HP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43406-0099-1MOTION SICKNESS HP30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43406-0099MOTION SICKNESS HP (ARNICA MONTANA, BRYONIA ALBA ROOT, QUININE SULFATE, ANAMIRTA COCCULUS SEED, CONIUM MACULATUM FLOWERING TOP, STRYCHNOS IGNATII SEED, IPECAC, POTASSIUM CARBONATE, STRYCHNOS NUX-VOMICA SEED, SEPIA OFFICINALIS JUICE, TOBACCO LEAF, VERATRUM ALBUM ROOT) LIQUID [NATURAL CREATIONS, INC.]2Current NDC, Legacy NDC, 1 package rows20230120_61da7048-b9a9-4af1-b1fc-c30dbaa66f1b.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ANAMIRTA COCCULUS SEEDACTIVE INGREDIENT810258W28U1
ARNICA MONTANAACTIVE INGREDIENTO80TY208ZW1
BRYONIA ALBA ROOTACTIVE INGREDIENTT7J046YI2B1
CONIUM MACULATUM FLOWERING TOPACTIVE INGREDIENTQ28R5GF3711
IPECACACTIVE INGREDIENT62I3C8233L1
POTASSIUM CARBONATEACTIVE INGREDIENTBQN1B9B9HA1
QUININE SULFATEACTIVE INGREDIENTKF7Z0E0Q2B1
SEPIA OFFICINALIS JUICEACTIVE INGREDIENTQDL83WN8C21
STRYCHNOS IGNATII SEEDACTIVE INGREDIENT1NM3M2487K1
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH139191
TOBACCO LEAFACTIVE INGREDIENT6YR2608RSU1
VERATRUM ALBUM ROOTACTIVE INGREDIENTQNS6W5US1Z1
ANAMIRTA COCCULUS SEEDACTIVE MOIETY810258W28U1
ARNICA MONTANAACTIVE MOIETYO80TY208ZW1
BRYONIA ALBA ROOTACTIVE MOIETYT7J046YI2B1
CARBONATE IONACTIVE MOIETY7UJQ5OPE7D1
CONIUM MACULATUM FLOWERING TOPACTIVE MOIETYQ28R5GF3711
IPECACACTIVE MOIETY62I3C8233L1
QUININEACTIVE MOIETYA7V27PHC7A1
SEPIA OFFICINALIS JUICEACTIVE MOIETYQDL83WN8C21
STRYCHNOS IGNATII SEEDACTIVE MOIETY1NM3M2487K1
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH139191
TOBACCO LEAFACTIVE MOIETY6YR2608RSU1
VERATRUM ALBUM ROOTACTIVE MOIETYQNS6W5US1Z1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43406-009943406-0099-1

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
ARNICA MONTANAO80TY208ZWACTIB
BRYONIA ALBA ROOTT7J046YI2BACTIB
QUININE SULFATEKF7Z0E0Q2BACTIB
ANAMIRTA COCCULUS SEED810258W28UACTIB
CONIUM MACULATUM FLOWERING TOPQ28R5GF371ACTIB
STRYCHNOS IGNATII SEED1NM3M2487KACTIB
IPECAC62I3C8233LACTIB
POTASSIUM CARBONATEBQN1B9B9HAACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
SEPIA OFFICINALIS JUICEQDL83WN8C2ACTIB
TOBACCO LEAF6YR2608RSUACTIB
VERATRUM ALBUM ROOTQNS6W5US1ZACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 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
MOTION SICKNESS HPARNICA MONTANA, BRYONIA ALBA ROOT, QUININE SULFATE, ANAMIRTA COCCULUS SEED, CONIUM MACULATUM FLOWERING TOP, STRYCHNOS IGNATII SEED, IPECAC, POTASSIUM CARBONATE, STRYCHNOS NUX-VOMICA SEED, SEPIA OFFICINALIS JUICE, TOBACCO LEAF, VERATRUM ALBUM ROOTNatural Creations, Inc.61da7048-b9a9-4af1-b1fc-c30dbaa66f1b2023-01-03WarningsExact identifier
ndc (package): 43406-0099-1
ndc (product): 43406-0099
ndc11 (package): 43406009901
spl id: 2779f075-075c-413a-b4a9-e8e0f4c2d586
spl set id: 61da7048-b9a9-4af1-b1fc-c30dbaa66f1b

Reported adverse events (FAERS/openFDA)#

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