FDA.reportPublic FDA data

GoPatch Motion Sickness and Dizziness Relief

Manufacturer
Centered Enterprises, LLC
Effective date
2024-01-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:25:41

Label at a glance#

ProductGoPatch Motion Sickness and Dizziness Relief
Active ingredientCALENDULA OFFICINALIS FLOWERING TOP, MATRICARIA RECUTITA, SEPIA OFFICINALIS JUICE, TOBACCO LEAF, ANAMIRTA COCCULUS SEED, STRYCHNOS NUX-VOMICA SEED
Label structure14 sections

Indications and uses

Uses* Temporarily relieves the symptoms of: ■ nausea and dizziness aggravated by motion from sea, car, air sickness, as well as motion sickness induced by theme park rides. ■ dizziness and vertigo

Dosage and administration

Directions ■ For best results apply GoPatch efore engaging in activities which promote motion sickness. ■ Can apply GoPatch after motion sickness has started. ■ To relieve dizziness or vertigo, apply GoPatch at onset of symptoms or before engaging in activities that create symptoms. ■ GoPatch must completely cover the navel. Skin around navel must be clean, dry & free of lotions. ■ Remove GoPatch from sheet and ap...

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredientsPurpose*
Cocculus Indicus 15C HPUS

relieves nausea, vomiting, dizziness

Nux Vomica 15C HPUS

relieves upset stomach, vertigo, headache

Tabacum 6C HPUS relieves headache & nausea; vomiting from motion
Sepia 3C HPUSrelieves dizziness & nausea accompanied by headache
Calendula Officinalis 3X HPUSsoothes skin
Chamomilla 3X HPUScalms sensitive skin

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*

Cocculus Indicus - relieves nausea, vomiting, dizziness

Nux Vomica - relieves upset stomach, vertigo, headache

Tabacum - relieves headache & nausea; vomiting from motion

Sepia - relieves dizziness & nausea accompanied by headache

Calendula Officinalis - soothes skin

Chamomilla - calms sensitive skin

Uses

INDICATIONS & USAGE SECTION

Uses*

Temporarily relieves the symptoms of: ■ nausea and dizziness aggravated by motion from sea, car, air sickness, as well as motion sickness induced by theme park rides.

■ dizziness and vertigo

WARNINGS SECTION

Warnings

  • For external use only.

Do Not Use

OTC - DO NOT USE SECTION

Do not use

■ on wounds, broken, or irritated skin
■ if you have had reactions to adhesives

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if fever develops, diarrhea lasts for more than 2 days or worsens, other symptoms persist for more than 3 days.

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

Ask Doctor

OTC - ASK DOCTOR SECTION

Ask doctor before use in children under 2 years of age.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

■ For best results apply GoPatch efore engaging in activities which promote motion sickness.

■ Can apply GoPatch after motion sickness has started.

■ To relieve dizziness or vertigo, apply GoPatch at onset of symptoms or before engaging in activities that create symptoms.

■ GoPatch must completely cover the navel. Skin around navel must be clean, dry & free of lotions.
■ Remove GoPatch from sheet and apply completely covering navel.
■ Remove GoPatch no more than 12 hours after application.

OTHER SAFETY INFORMATION

Other information

  • Store out of direct sunlight, in dry place, at 65-80°F (20-25°C).
  • Contains no known allergens, free of latex, corn, soy, wheat, and yeast.
  • If unsatisfied with GoPatch, please email us at WeCare@TheGoPatch.com for full money back guarantee.

INACTIVE INGREDIENT SECTION

Inactive ingredients Acrylic adhesive

Questions?

OTC - QUESTIONS SECTION

Questions or comments? Please call us at (707) 733-3011 or www.TheGoPatch.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GoPatch™

NDC 70105-003-05

Homeopathic

LabelLabel

LabelLabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70105-003-05GoPatch Motion Sickness and Dizziness Relief5 in 1 BOXPATCH52

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70105-003GOPATCH MOTION SICKNESS AND DIZZINESS RELIEF (CALENDULA OFFICINALIS, CHAMOMILLA, SEPIA, TABACUM, COCCULUS INDICUS, NUX VOMICA) PATCH [CENTERED ENTERPRISES, LLC]2Current NDC, Legacy NDC, 1 package rows20240116_c4730e15-20e0-37fa-e053-2a95a90a6181.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70105-00370105-003-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYVINYL ACETATE32K497ZK2UIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
CALENDULA OFFICINALIS FLOWERING TOP18E7415PXQACTIB
MATRICARIA RECUTITAG0R4UBI2ZZACTIB
SEPIA OFFICINALIS JUICEQDL83WN8C2ACTIB
TOBACCO LEAF6YR2608RSUACTIB
ANAMIRTA COCCULUS SEED810258W28UACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB

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
GoPatch Motion Sickness and Dizziness ReliefCALENDULA OFFICINALIS, CHAMOMILLA, SEPIA, TABACUM, COCCULUS INDICUS, NUX VOMICACentered Enterprises, LLCc4730e15-20e0-37fa-e053-2a95a90a61812024-01-15WarningsExact identifier
ndc (package): 70105-003-05
ndc (product): 70105-003
ndc11 (package): 70105000305
spl id: 0f04ad8c-da5e-5708-e063-6394a90a6d90
spl set id: c4730e15-20e0-37fa-e053-2a95a90a6181

Reported adverse events (FAERS/openFDA)#

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