Dizzy

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2024-03-15
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:26:23

Label at a glance#

ProductDizzy
Active ingredientSUS SCROFA CEREBRUM, BRYONIA ALBA ROOT, KEROSENE, TOBACCO LEAF, AMBERGRIS, CYCLAMEN PURPURASCENS TUBER, SODIUM SALICYLATE, SILVER NITRATE, ASARUM CANADENSE ROOT, CALCIUM SULFATE ANHYDROUS, CARBON DISULFIDE, QUININE SULFATE, ANAMIRTA COCCULUS SEED, CONIUM MACULATUM FLOWERING TOP, DIGITALIS, GELSEMIUM SEMPERVIRENS ROOT, PHOSPHORUS, MACROPIPER METHYSTICUM ROOT, SILICON DIOXIDE, THERIDION CURASSAVICUM
Label structure9 sections

Indications and uses

• For the temporary relief of symptoms including: • vertigo • faintness • vomiting • motion sickness  • spinning or swaying • weakness These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Dosage and administration

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Ambra Grisea 9X, Argentum Nitricum 12X, Asarum Canadense 12X, Bryonia (Alba) 8X, Calcarea Sulphurica 12X, Carboneum Sulphuratum 12X, Cerebellum (Suis) 6X, 12X, 30X, 200X, Chininum Sulphuricum 12X, Cocculus Indicus 12X, Conium Maculatum 12X, Cyclamen Europaeum 9X, Digitalis Purpurea 12X, Gelsemium Sempervirens 12X, Natrum Salicylicum 10X, Petroleum 8X, Phosphorus 12X, Piper Methysticum 12X, Silicea 12X, Tabacum 8X, Theridion 12X.

PURPOSE:

OTC - PURPOSE SECTION

Ambra Grisea - Vertigo, Argentum Nitricum - Faintness, Asarum Canadense - Vomiting, Bryonia (Alba) – Motion Sickness, Calcarea Sulphurica - Weakness, Carboneum Sulphuratum – Spinning or Swaying, Cerebellum (Suis) - Vertigo, Chininum Sulphuricum -
Faintness, Cocculus Indicus - Vomiting, Conium Maculatum – Motion Sickness, Cyclamen Europaeum - Weakness, Digitalis Purpurea – Spinning or Swaying, Gelsemium Sempervirens - Vertigo, Natrum Salicylicum - Faintness, Petroleum - Vomiting, Phosphorus – Motion Sickness, Piper Methysticum - Weakness, Silicea – Spinning or Swaying, Tabacum - Faintness, Theridion - Vertigo

USES:

INDICATIONS & USAGE SECTION

• For the temporary relief of symptoms including:

• vertigo • faintness • vomiting • motion sickness

 • spinning or swaying • weakness

These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

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

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

Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, contact a physician or Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 25% ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By: Deseret Biologicals, Inc.
469 W. Parkland Drive
Sandy, UT 84070

www.desbio.co

800-827-8204

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DesBio

Dizzy

Homeopathic

NDC 43742-1675-1

1 FL OZ (30 ml)

DizzyDizzy

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
22bca8fc-c2b1-897d-b515-117a7522ccaeProduct name320150731
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43742-1675-1Dizzy30 mL in 1 BOTTLE, DROPPERLIQUID304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-1675DIZZY (CEREBELLUM (SUIS), BRYONIA (ALBA), PETROLEUM, TABACUM, AMBRA GRISEA, CYCLAMEN EUROPAEUM, NATRUM SALICYLICUM, ARGENTUM NITRICUM, ASARUM CANADENSE, CALCAREA SULPHURICA, CARBONEUM SULPHURATUM, CHININUM SULPHURICUM, COCCULUS INDICUS, CONIUM MACULATUM, DIGITALIS PURPUREA, GELSEMIUM SEMPERVIRENS, PHOSPHORUS, PIPER METHYSTICUM, SILICEA, THERIDION) LIQUID [DESERET BIOLOGICALS, INC.]4Current NDC, Legacy NDC, 1 package rows20240317_fdf934f8-7b12-4076-b8fb-00c095940697.zip

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-167543742-1675-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 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
DizzyCEREBELLUM (SUIS), BRYONIA (ALBA), PETROLEUM, TABACUM, AMBRA GRISEA, CYCLAMEN EUROPAEUM, NATRUM SALICYLICUM, ARGENTUM NITRICUM, ASARUM CANADENSE, CALCAREA SULPHURICA, CARBONEUM SULPHURATUM, CHININUM SULPHURICUM, COCCULUS INDICUS, CONIUM MACULATUM, DIGITALIS PURPUREA, GELSEMIUM SEMPERVIRENS, PHOSPHORUS, PIPER METHYSTICUM, SILICEA, THERIDIONDeseret Biologicals, Inc.fdf934f8-7b12-4076-b8fb-00c0959406972024-03-15WarningsExact identifier
ndc (package): 43742-1675-1
ndc (product): 43742-1675
ndc11 (package): 43742167501
spl id: 7581a689-8459-41c1-8546-c99d733347ad
spl set id: fdf934f8-7b12-4076-b8fb-00c095940697

Reported adverse events (FAERS/openFDA)#

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