WellMind Vertigo

Manufacturer
MediNatura Inc.
Effective date
2023-04-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:20:55

Label at a glance#

ProductWellMind Vertigo
Active ingredientSEMECARPUS ANACARDIUM JUICE, ANAMIRTA COCCULUS SEED, CONIUM MACULATUM FLOWERING TOP, PETROLEUM ALKYLATE, SELENIUM
Label structure8 sections

Dosage and administration

Adults and children 12 years and older: 1-2 tablets 3 times per day or as directed by a health practitioner. Not to exceed 6 tablets per 24 hours. Children under 12, as directed by a health professional. Allow to completely dissolve in the mouth

Label contents#

Full prescribing information#

Warnings:

WARNINGS SECTION

 If pregnant or breast-feeding, ask
a health professional before use. Keep out of
reach of children. If symptoms persist or worsen,
a healthcare provider should be consulted. Do not
use if known sensitivity to WellMind Vertigo® or any
of its ingredients exists.

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Each 300 mg tablet contains:
*Anacardium orientale 6X 10mg, *Cocculus indicus
4X 210mg, *Conium maculatum 3X 30mg,
*Petroleum 8X 20mg, *Selenium metallicum 6X
10mg, *Selenium metallicum 12X 10mg, *Selenium
metallicum 30X 10mg. *Natural

Inactive ingredients:

INACTIVE INGREDIENT SECTION

*Dextrose, *Lactose,
Magnesium stearate, *Maltodextrin
*contains one or more of these ingredients

Purpose

OTC - PURPOSE SECTION

Motion Sickness
Relief

Directions:

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years and
older: 1-2 tablets 3 times per day or as directed by a
health practitioner. Not to exceed 6 tablets per 24
hours. Children under 12, as directed by a health
professional. Allow to completely dissolve in the mouth

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Indications:

INDICATIONS & USAGE SECTION

For the temporary relief of minor
lightheadedness and motion sickness.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WellMind Vertigo.jpgWellMind Vertigo.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
86fffa7b-d382-4771-a253-25cccb64b590Product name320251124
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62795-9003-22025-01-30C16284748780-12cef2736-8236-d83d-e063-dadaa90ab31fWellMind Vertigo

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62795-9003-2WellMind Vertigo1 in 1 CARTONTABLET12
62795-9003-2WellMind Vertigo100 in 1 BOTTLETABLET1002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62795-9003WELLMIND VERTIGO (SEMECARPUS ANACARDIUM JUICE, ANAMIRTA COCCULUS SEED, CONIUM MACULATUM FLOWERING TOP, KEROSENE, AND SELENIUM) TABLET [MEDINATURA INC.]2Legacy NDC, 2 package rows20230420_79f538e2-6c1b-4c6d-8d04-0283db4c965f.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
62795-9003-2EA - Each62795-9003beafa65e-f9f7-4270-9119-8a0cdb2ec93a12022-05-04

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
62795-900362795-9003-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
6fca3c42-3180-4925-be6d-0e60b30abb3079f538e2-6c1b-4c6d-8d04-0283db4c965f2023-04-19WarningsExact identifier
spl id: 6fca3c42-3180-4925-be6d-0e60b30abb30
spl set id: 79f538e2-6c1b-4c6d-8d04-0283db4c965f

Reported adverse events (FAERS/openFDA)#

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