Vertitone

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-10-31
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:28:41

Label at a glance#

ProductVertitone
Active ingredientBAPTISIA TINCTORIA ROOT, AMANITA MUSCARIA FRUITING BODY, ARSENIC TRIOXIDE, ATROPA BELLADONNA, OYSTER SHELL CALCIUM CARBONATE, CRUDE, ANAMIRTA COCCULUS SEED, CONIUM MACULATUM FLOWERING TOP, PHOSPHORUS, PULSATILLA PRATENSIS WHOLE
Label structure9 sections

Dosage and administration

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(in each drop): 12.49% of Agaricus Muscarius 12X, Arsenicum Album 12X, Belladonna 12X, Calcarea Carbonica 12X, Cocculus Indicus 12X, Conium Maculatum 12X, Phosphorus 12X, Pulsatilla (Pratensis) 12X; 0.10% of Baptisia Tinctoria 3X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve dizziness and motion sickness with nausea.**

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

WARNINGS:

WARNINGS SECTION

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

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve dizziness and motion sickness with nausea.**

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

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 20% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by Energique, Inc.

201 Apple Blvd

Woodbine, IA 51579   800.869.8078

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

VERTITONE

1 fl. oz. (30 ml)

VertitoneVertitone

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0181-12024-10-31C16284748780-1d6a99b39-fe7d-a426-e053-dadaa90af4c2DRUG FACTS:
44911-0181-12024-01-30C16284748780-1d6a99b39-fe7d-a426-e053-dadaa90af4c2DRUG FACTS:
44911-0181-12022-05-20C16284748780-1d6a99b39-fe7d-a426-e053-dadaa90af4c2DRUG FACTS:
44911-0181-12022-01-28C16284748780-1d6a99b39-fe7d-a426-e053-dadaa90af4c2DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0181-1Vertitone30 mL in 1 BOTTLE, DROPPERLIQUID305

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0181VERTITONE (BAPTISIA TINCTORIA, AGARICUS MUSCARIUS, ARSENICUM ALBUM, BELLADONNA, CALCAREA CARBONICA, COCCULUS INDICUS, CONIUM MACULATUM, PHOSPHORUS, PULSATILLA (PRATENSIS)) LIQUID [ENERGIQUE, INC.]5Current NDC, Legacy NDC, 1 package rows20241102_12f1c465-b64a-446c-a28c-e96dabe03580.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AMANITA MUSCARIA FRUITING BODYACTIVE INGREDIENTDIF093I0371
ANAMIRTA COCCULUS SEEDACTIVE INGREDIENT810258W28U1
ARSENIC TRIOXIDEACTIVE INGREDIENTS7V92P67HO1
ATROPA BELLADONNAACTIVE INGREDIENTWQZ3G9PF0H1
BAPTISIA TINCTORIA ROOTACTIVE INGREDIENT5EF0HWI5WU1
CONIUM MACULATUM FLOWERING TOPACTIVE INGREDIENTQ28R5GF3711
OYSTER SHELL CALCIUM CARBONATE, CRUDEACTIVE INGREDIENT2E32821G6I1
PHOSPHORUSACTIVE INGREDIENT27YLU75U4W1
PULSATILLA PRATENSISACTIVE INGREDIENT8E272251DI1
AMANITA MUSCARIA FRUITING BODYACTIVE MOIETYDIF093I0371
ANAMIRTA COCCULUS SEEDACTIVE MOIETY810258W28U1
ARSENIC CATION (3+)ACTIVE MOIETYC96613F5AV1
ATROPA BELLADONNAACTIVE MOIETYWQZ3G9PF0H1
BAPTISIA TINCTORIA ROOTACTIVE MOIETY5EF0HWI5WU1
CONIUM MACULATUM FLOWERING TOPACTIVE MOIETYQ28R5GF3711
OYSTER SHELL CALCIUM CARBONATE, CRUDEACTIVE MOIETY2E32821G6I1
PHOSPHORUSACTIVE MOIETY27YLU75U4W1
PULSATILLA PRATENSISACTIVE MOIETY8E272251DI1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-018144911-0181-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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 · 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
VertitoneBAPTISIA TINCTORIA, AGARICUS MUSCARIUS, ARSENICUM ALBUM, BELLADONNA, CALCAREA CARBONICA, COCCULUS INDICUS, CONIUM MACULATUM, PHOSPHORUS, PULSATILLA (PRATENSIS)Energique, Inc.12f1c465-b64a-446c-a28c-e96dabe035802024-10-31WarningsExact identifier
ndc (package): 44911-0181-1
ndc (product): 44911-0181
ndc11 (package): 44911018101
spl id: 2f9df577-5024-4911-9ab7-ad3387dff794
spl set id: 12f1c465-b64a-446c-a28c-e96dabe03580

Reported adverse events (FAERS/openFDA)#

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