Dizziness

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2025-11-19
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:35:16

Label at a glance#

ProductDizziness HP
Active ingredientOYSTER SHELL CALCIUM CARBONATE, CRUDE, DYSPHANIA AMBROSIOIDES, ANAMIRTA COCCULUS SEED, CONIUM MACULATUM FLOWERING TOP, STRYCHNOS NUX-VOMICA SEED, PHOSPHORUS, PULSATILLA PRATENSIS WHOLE, SILICON DIOXIDE, TOBACCO LEAF
Label structure9 sections

Dosage and administration

Adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional. If symptoms persist, 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): 11.11% of Calcarea Carbonica 30X, Chenopodium Anthelminticum 30X, Cocculus Indicus 30X, Conium Maculatum 30X, Nux Vomica 30X, Phosphorus 30X, Pulsatilla (Pratensis)30X, Silicea 30X, Tabacum 30X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms of dizziness and light-headedness.**

**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, 1 time daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional.

Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve symptoms of dizziness and light-headedness.**

**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

DIZZINESS HP

1 fl. oz. (30 ml)

DIZZINESS HPDIZZINESS HP

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0187-12025-11-19C16284748780-11030e365-1511-111a-e063-dadaa90a10e2DRUG FACTS:
44911-0187-12024-01-30C16284748780-11030e365-1511-111a-e063-dadaa90a10e2DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0187-1DizzinessHP30 mL in 1 BOTTLE, DROPPERLIQUID305

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ANAMIRTA COCCULUS SEEDACTIVE INGREDIENT810258W28U1
CONIUM MACULATUM FLOWERING TOPACTIVE INGREDIENTQ28R5GF3711
DYSPHANIA AMBROSIOIDESACTIVE INGREDIENT4H5RSU087I1
OYSTER SHELL CALCIUM CARBONATE, CRUDEACTIVE INGREDIENT2E32821G6I1
PHOSPHORUSACTIVE INGREDIENT27YLU75U4W1
PULSATILLA PRATENSISACTIVE INGREDIENT8E272251DI1
SILICON DIOXIDEACTIVE INGREDIENTETJ7Z6XBU41
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH139191
TOBACCO LEAFACTIVE INGREDIENT6YR2608RSU1
ANAMIRTA COCCULUS SEEDACTIVE MOIETY810258W28U1
CHENOPODIUM AMBROSIOIDESACTIVE MOIETY4H5RSU087I1
COLLOIDAL SILICON DIOXIDEACTIVE MOIETYETJ7Z6XBU41
CONIUM MACULATUM FLOWERING TOPACTIVE MOIETYQ28R5GF3711
OYSTER SHELL CALCIUM CARBONATE, CRUDEACTIVE MOIETY2E32821G6I1
PHOSPHORUSACTIVE MOIETY27YLU75U4W1
PULSATILLA PRATENSISACTIVE MOIETY8E272251DI1
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH139191
TOBACCO LEAFACTIVE MOIETY6YR2608RSU1
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
44911-018744911-0187-1

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
Dizziness HPCALCAREA CARBONICA, CHENOPODIUM ANTHELMINTICUM, COCCULUS INDICUS, CONIUM MACULATUM, NUX VOMICA, PHOSPHORUS, PULSATILLA (PRATENSIS), SILICEA, TABACUM,Energique, Inc.0bf53ecc-c2ad-40b5-b921-7c10a1b006262025-11-19WarningsExact identifier
ndc (package): 44911-0187-1
ndc (product): 44911-0187
ndc11 (package): 44911018701
spl id: f02fda13-544f-409a-bb7b-038d49cf4932
spl set id: 0bf53ecc-c2ad-40b5-b921-7c10a1b00626

Reported adverse events (FAERS/openFDA)#

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