Dosage and administration
Dissolve 1-2 tablets under the tongue as needed. Children 2-12 years old: 1/2 adult dose.
Vertaway
- Manufacturer
- HelloLife, Inc. | Apotheca Company
- Effective date
- 2020-01-21
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 5
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 23:43:51
Label at a glance#
ProductVertaway
Active ingredientAMYL NITRITE, THYROID, BOVINE, SILVER NITRATE, BRYONIA ALBA ROOT, CALENDULA OFFICINALIS FLOWERING TOP, ANAMIRTA COCCULUS SEED, NITROGLYCERIN, SKIM MILK, STRYCHNOS NUX-VOMICA SEED, KEROSENE, TOBACCO LEAF, ATROPA BELLADONNA, THERIDION CURASSAVICUM, WATER
Label structure9 sections
Contacts and useful links#
Websitewww.hellolife.net
www.hellolife.net
www.hellolife.netLabel contents#
Full prescribing information#
ACTIVE HPUS INGREDIENTS:
Amyl Nitrosum 6X, Thyroidinum (Bovine) 6X, 30X, Argentum Nitricum 6X, 30X, 1LM, Bryonia (Alba) 6X, 30X, 1LM, Calendula Officinalis 6X, 30X, 1LM, Cocculus Indicus 6X, 30X, 1LM, Glonoinum 6X, 30X, 1LM, Lac Defloratum 6X, 30X, 1LM, Nux Vomica 6X, 30X, 1LM, Petroleum 6X, 30X, 1LM, Tabacum 6X, 30X, 1LM, Belladonna 10X, 30X, 1LM, Theridion 30X, 1LM, Sanicula 30X, 5LM.
The letters "HPUS" indicated that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.
INDICATIONS FOR USE:
For the temporary relief of symptoms commonly associated with vertigo and/or motion sickness such as dizziness, headache, nausea, vomiting, and faintness on rising.
Product indications based on Homeopathic Materia Medica for self-limiting conditions.
WARNINGS:
If symptoms persist or worsen, seek advice of a physician.
If pregnant or breast-feeding, take only on advice of a physician.
In case of overdose, get medical help or contact a Poison Control Center right away.
Do not use if tamper seal is broken.
Keep out of reach of children.
Storage and Handling
Do not store next to electrical devices or appliances.
Keep lid tightly closed and store in a cool, dry place.
KEEP OUT OF REACH OF CHILDREN:
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
DIRECTIONS:
Dissolve 1-2 tablets under the tongue as needed.
Children 2-12 years old: 1/2 adult dose.
INDICATIONS FOR USE:
For the temporary relief of symptoms commonly associated with vertigo and/or motion sickness such as dizziness, headache, nausea, vomiting, and faintness on rising.
Product indications based on Homeopathic Materia Medica for self-limiting conditions.
INACTIVE INGREDIENTS:
Advantol 300, lactose, magnesium stearate, mannitol, microcrystalline cellulose, no gluten added.
QUESTIONS:
Mftd for: HelloLife, Inc.
4460 44th St SE, Ste C-600
Grand Rapids, MI 49512
Call us tool-free at: 1-800-875-0850 or
visit us on the web at www.hellolife.net
PACKAGE LABEL DISPLAY:
NDC 49726-037-90
VertAway
Vertigo Symptom Relief
Homeopathic (OTC) Medicine
90 Quick-dissolving Tablets
Products#
Every source-derived product name is available through these pages.
- Vertaway
- Amyl Nitrosum, Thyroidinum (Bovine), Argentum Nitricum, Bryonia (Alba), Calendula Officinalis, Cocculus Indicus, Glonoinum, Lac Defloratum, Nux Vomica, Petroleum, Tabacum, Belladonna, Theridion, Sanicula
- AMYL NITRITE
- THYROID, BOVINE
- SILVER NITRATE
- SILVER CATION
- BRYONIA ALBA ROOT
- CALENDULA OFFICINALIS FLOWERING TOP
- ANAMIRTA COCCULUS SEED
- NITROGLYCERIN
- SKIM MILK
- STRYCHNOS NUX-VOMICA SEED
- KEROSENE
- TOBACCO LEAF
- ATROPA BELLADONNA
- THERIDION CURASSAVICUM
- WATER
- LACTOSE
- MAGNESIUM STEARATE
- MANNITOL
- CELLULOSE, MICROCRYSTALLINE
- SORBITOL
- SILICON DIOXIDE
- CROSPOVIDONE
- COPOVIDONE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 49726-037 | 49726-037-90 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| b3420046-8164-4f3f-a5d4-9697d107c000 | 120b93ce-faab-4610-8d9d-1e773323fd32 | 2016-06-21 | Warnings | 120b93ce-faab-4610-8d9d-1e773323fd32 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.