Motion Sickness

Manufacturer
Newton Laboratories, Inc.
Effective date
2011-03-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:05:01

Label at a glance#

ProductMotion Sickness
Active ingredientWormwood, Aconitum Napellus, Antimony Potassium Tartrate, Atropa Belladonna, Bryonia Alba Root, Phenol, Colchicum Autumnale Bulb, Conium Maculatum Flowering Top, Iron, Gelsemium Sempervirens Root, Nitroglycerin, Hyoscyamus Niger, Ipecac, Iris Versicolor Root, Lycopodium Clavatum Spore, Strychnos Nux-vomica Seed, Kerosene, Phosphorus, Sepia Officinalis Juice, Symphoricarpos Albus Fruit, Tobacco Leaf, Theridion Curassavicum, Ginger, Echinacea, Unspecified, Hypericum Perforatum, Passiflora Incarnata Flowering Top, Valerian
Label structure10 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Motion Sickness    Formulated for associated symptoms of the effects or the sensation of movement such as dizziness, discomfort, headache, nausea and disorientation.

DOSAGE & ADMINISTRATION SECTION

Directions:   Ages 12 and up, take 6 pellets orally (ages 0 to 11, give 3 pellets) as needed or as directed by a healthcare professional. Under age 2, crush or dissolve pellets in purified water.  Sensitive persons begin with 1 pellet and gradually increase to full dose.

OTC - ACTIVE INGREDIENT SECTION

Absinthium 15x, Aconitum nap. 15x, Antimon. tart. 15x, Belladonna 15x, Bryonia 15x, Carbolicum acidum 15x, Colchicum 15x, Conium 15x, Ferrum metallicum 15x, Gelsemium 15x, Glonoinum 15x, Hyoscyamus 15x, Ipecac. 15x, Iris versicolor 15x, Lycopodium 15x, Nux vom. 15x, Petroleum 15x, Phosphorus 15x, Sepia 15x, Symphoricarpus racemosus 15x, Tabacum 15x, Theridion 15x, Zingiber 15x, Echinacea 3x, Hypericum 3x, Passiflora 3x, Valeriana 3x.

OTC - PURPOSE SECTION

Formulated for associated symptoms of the effects or the sensation of movement such as dizziness, discomfort, headache, nausea and disorientation.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Gluten-free, non-GMO, beet-derived sucrose pellets.

QUESTIONS SECTION

OTC - QUESTIONS SECTION

www.newtonlabs.net  Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30012
Questions?  1.800.448.7256 

WARNINGS SECTION

Warning: Do not use if tamper - evident seal is broken or missing. Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days. Keep out of reach of children.  

OTC - PREGNANCY OR BREAST FEEDING SECTION

Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days. 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label
package label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7480e90b-004b-ebe4-2243-4f2fefdd9e78Product name220260128
3f158398-73f2-4b90-47d1-5c60e8719a98Product name920250721
ca6149a6-ded3-9f17-6c41-3e88f2c0c9c0Product name220250117
910c1bd7-67d1-44c7-ad4f-9445f827edccProduct name120230808
00358076-c817-430b-b924-11d717dc307cProduct name120160718
669af5aa-14f3-3df7-f100-5f580ffd43c1Product name120140508
6ff3bab7-2dce-8bea-d7ce-54687f0c01fbProduct name120140508
8bb82a1c-d0d0-fc27-011f-172e545f0382Product name120140508
cb03406d-e223-80bb-67d8-be80f9b6a4f2Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55714-2289-02020-01-31C16284748780-19d75b9cf-d448-f424-e053-dadaa90a57ceMotion Sickness
55714-2289-12020-01-31C16284748780-19d75b9cf-d448-f424-e053-dadaa90a57ceMotion Sickness
55714-2289-22020-01-31C16284748780-19d75b9cf-d448-f424-e053-dadaa90a57ceMotion Sickness

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55714-2289-0Motion Sickness7.08 g in 1 BOTTLE, GLASSPELLET7.081
55714-2289-1Motion Sickness28.35 g in 1 BOTTLE, GLASSPELLET28.351
55714-2289-2Motion Sickness56.7 g in 1 BOTTLE, GLASSPELLET56.71

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55714-2289MOTION SICKNESS (ABSINTHIUM, ACONITUM NAP., ANTIMON. TART., BELLADONNA, BRYONIA, CARBOLICUM ACIDUM, COLCHICUM, CONIUM, FERRUM METALLICUM, GELSEMIUM, GLONOINUM, HYOSCYAMUS, IPECAC., IRIS VERSICOLOR, LYCOPODIUM, NUX VOM., PETROLEUM, PHOSPHORUS, SEPIA, SYMPHORICARPUS RACEMOSUS, TABACUM, THERIDION, ZINGIBER, ECHINACEA, HYPERICUM, PASSIFLORA, VALERIANA) PELLET [NEWTON LABORATORIES, INC.]1Legacy NDC, 3 package rows20131016_4bc132ba-c052-4001-4347-e49667d32ed4.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Aconitum NapellusACTIVE INGREDIENTU0NQ8555JD1
Antimony Potassium TartrateACTIVE INGREDIENTDL6OZ476V31
Atropa BelladonnaACTIVE INGREDIENTWQZ3G9PF0H1
Bryonia Alba RootACTIVE INGREDIENTT7J046YI2B1
Colchicum Autumnale BulbACTIVE INGREDIENT993QHL78E61
Conium Maculatum Flowering TopACTIVE INGREDIENTQ28R5GF3711
Echinacea, UnspecifiedACTIVE INGREDIENT4N9P6CC1DX1
Gelsemium Sempervirens RootACTIVE INGREDIENT639KR60Q1Q1
GingerACTIVE INGREDIENTC5529G5JPQ1
Hyoscyamus NigerACTIVE INGREDIENT4WRK2153H31
Hypericum PerforatumACTIVE INGREDIENTXK4IUX8MNB1
IpecacACTIVE INGREDIENT62I3C8233L1
Iris Versicolor RootACTIVE INGREDIENTX43D4L3DQC1
IronACTIVE INGREDIENTE1UOL152H71
KeroseneACTIVE INGREDIENT1C89KKC04E1
Lycopodium Clavatum SporeACTIVE INGREDIENTC88X29Y4791
NitroglycerinACTIVE INGREDIENTG59M7S0WS31
Passiflora Incarnata Flowering TopACTIVE INGREDIENTCLF5YFS11O1
PhenolACTIVE INGREDIENT339NCG44TV1
PhosphorusACTIVE INGREDIENT27YLU75U4W1
Sepia Officinalis JuiceACTIVE INGREDIENTQDL83WN8C21
Strychnos Nux-vomica SeedACTIVE INGREDIENT269XH139191
Symphoricarpos Albus FruitACTIVE INGREDIENT873JZU3ASZ1
Theridion CurassavicumACTIVE INGREDIENT9Z8D3HEM8L1
Tobacco LeafACTIVE INGREDIENT6YR2608RSU1
ValerianACTIVE INGREDIENTJWF5YAW3QW1
WormwoodACTIVE INGREDIENTF84709P2XV1
Aconitum NapellusACTIVE MOIETYU0NQ8555JD1
Antimony Cation (3+)ACTIVE MOIETY069647RPT51
Atropa BelladonnaACTIVE MOIETYWQZ3G9PF0H1
Bryonia Alba RootACTIVE MOIETYT7J046YI2B1
Colchicum Autumnale BulbACTIVE MOIETY993QHL78E61
Conium Maculatum Flowering TopACTIVE MOIETYQ28R5GF3711
Echinacea, UnspecifiedACTIVE MOIETY4N9P6CC1DX1
Gelsemium Sempervirens RootACTIVE MOIETY639KR60Q1Q1
GingerACTIVE MOIETYC5529G5JPQ1
Hyoscyamus NigerACTIVE MOIETY4WRK2153H31
Hypericum PerforatumACTIVE MOIETYXK4IUX8MNB1
IpecacACTIVE MOIETY62I3C8233L1
Iris Versicolor RootACTIVE MOIETYX43D4L3DQC1
IronACTIVE MOIETYE1UOL152H71
KeroseneACTIVE MOIETY1C89KKC04E1
Lycopodium Clavatum SporeACTIVE MOIETYC88X29Y4791
NitroglycerinACTIVE MOIETYG59M7S0WS31
Passiflora Incarnata Flowering TopACTIVE MOIETYCLF5YFS11O1
PhenolACTIVE MOIETY339NCG44TV1
PhosphorusACTIVE MOIETY27YLU75U4W1
Sepia Officinalis JuiceACTIVE MOIETYQDL83WN8C21
Strychnos Nux-vomica SeedACTIVE MOIETY269XH139191
Symphoricarpos Albus FruitACTIVE MOIETY873JZU3ASZ1
Theridion CurassavicumACTIVE MOIETY9Z8D3HEM8L1
Tobacco LeafACTIVE MOIETY6YR2608RSU1
ValerianACTIVE MOIETYJWF5YAW3QW1
WormwoodACTIVE MOIETYF84709P2XV1
SucroseINACTIVE INGREDIENTC151H8M5541

Products#

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

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55714-228955714-2289-1, 55714-2289-2, 55714-2289-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 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 · 48 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
SucroseSUCROSEC151H8M554GRANULE, FOR SOLUTION / ORAL42596 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554LOZENGE / BUCCALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SUSPENSION / ORAL48209 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554LOZENGE / TRANSMUCOSAL1255 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, EMULSION / INTRAVENOUS970 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET / BUCCAL109 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SUPPOSITORY / RECTALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, FILM COATED, EXTENDED RELEASE / ORAL119.12 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, POWDER, FOR SUSPENSION / INTRAVENOUS900 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CONCENTRATE / ORAL4800 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, CHEWABLE / ORAL7258 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TROCHE / ORALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, EXTENDED RELEASE / ORAL284.54 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTABLE, LIPOSOMAL / INTRAVENOUS7560 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554DROPS / ORALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, FILM COATED / ORAL145 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554LIQUID / ORAL37500 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SUSPENSION/ DROPS / ORAL3750 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SUSPENSION, EXTENDED RELEASE / ORAL5400 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554ELIXIR / ORAL18000 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CAPSULE / ORAL3568 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CAPSULE, COATED, EXTENDED RELEASE / ORAL86 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554GRANULE / ORALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, DELAYED RELEASE / ORAL295.33 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554PASTILLE / ORAL426 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554POWDER / ORAL27768 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET / ORAL4249 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, COATED / ORAL516.42 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CAPSULE, EXTENDED RELEASE / ORAL619 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554POWDER, FOR SUSPENSION / ORAL40017 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554POWDER, FOR SOLUTION / ORAL38666 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, SOLUTION / INTRAVENOUSNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / SUBCUTANEOUS308 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET / SUBLINGUAL109 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554WAFER / ORAL155.2 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION / INTRAVENOUS1950 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION / SUBCUTANEOUS47.75 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554GRANULE, FOR SUSPENSION, EXTENDED RELEASE / ORAL18790 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554GRANULE, FOR SUSPENSION / ORAL31885 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, SUSPENSION, EXTENDED RELEASE / SUBCUTANEOUS1 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CAPSULE, DELAYED RELEASE / ORAL955 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CAPSULE, COATED PELLETS / ORAL59.8 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SOLUTION / ORAL70000 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SYRUP / ORAL46400 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, SUSPENSION, LIPOSOMAL / INTRAVENOUS9.4 %w/vExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SOLUTION / RECTAL35.42 %w/vExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TROCHE / BUCCALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS2000 mgExact identifier — unii candidate
48 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
ac0e970b-03d4-dd60-f39a-0b9a19de3a184bc132ba-c052-4001-4347-e49667d32ed42011-03-01WarningsExact identifier
spl id: ac0e970b-03d4-dd60-f39a-0b9a19de3a18
spl set id: 4bc132ba-c052-4001-4347-e49667d32ed4

Reported adverse events (FAERS/openFDA)#

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