FDA.reportPublic FDA data

DIZZINESS HP

Manufacturer
Natural Creations, Inc. | OHM Pharma, Inc.
Effective date
2025-12-10
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:35:45

Label at a glance#

ProductDIZZINESS HP
Active ingredientOYSTER SHELL CALCIUM CARBONATE, CRUDE, CHENOPODIUM AMBROSIOIDES, ANAMIRTA COCCULUS SEED, CONIUM MACULATUM FLOWERING TOP, STRYCHNOS NUX-VOMICA SEED, PHOSPHORUS, PULSATILLA VULGARIS, SILICON DIOXIDE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS (HPUS*) - equal amounts of: Calcarea Carbonica 30X, Cheopodium Anthelminticum 30X, Cocculus Indicus 30X, Conium Maculatum 30X, Nux Vomica 30X, Phosphorus 30X, Pulsatilla 30X, Silicea 30X

OTC - PURPOSE SECTION

USES: Temporarily relieves dizziness and nausea.**

INDICATIONS & USAGE SECTION

USES: Temporarily relieves dizziness and nausea.**

DOSAGE & ADMINISTRATION SECTION

Directions:  Adults & children above 12 years:  10 drops orally 3 times daily, or as directed by a health care professional.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF THE REACH OF CHILDREN.  In case of overdose (or accidental ingestion) get    medical help or contact a Poison Control Center right away

WARNINGS SECTION

WARNINGS:

  •   Consult a physician for use in children under 12 years of age.
  • IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use.
  • KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.
  • Do not use if TAMPER EVIDENT seal is broken or missing.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:  Purified Water, USP Ethanol Alcohol 20%

OTC - QUESTIONS SECTION

Questions & Comments?  Natural Creations, Inc. / Woodbine, IA 51579 / 712-647-1600

REFERENCES SECTION

*The  letters “HPUS” indicate the components in the product are officially monographed in the Homeopathic Pharmacopeia of the United States.

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 43406-0017-1

DIZZINESS HP

HOMEOPATHIC

1 fl oz (30 mL) 20% Alcohol

image of labelimage of label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130877730001245GTIN-13: 0877730001245
EAN-13: 0877730001245
GTIN-12: 877730001245
UPC-A: 877730001245
GTIN storage (14 digits): 00877730001245		DIZZINESS HP.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43406-0017-12023-01-19C16284748780-19855d018-d529-cd31-e053-dbdaa90ab51aDIZZINESS HP
43406-0017-12019-11-27C16284748780-19855d018-d529-cd31-e053-dbdaa90ab51aDIZZINESS HP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43406-0017-1DIZZINESS HP30 mL in 1 BOTTLE, DROPPERLIQUID304

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ANAMIRTA COCCULUS SEEDACTIVE INGREDIENT810258W28U1
CHENOPODIUM AMBROSIOIDESACTIVE INGREDIENT4H5RSU087I1
CONIUM MACULATUM FLOWERING TOPACTIVE INGREDIENTQ28R5GF3711
OYSTER SHELL CALCIUM CARBONATE, CRUDEACTIVE INGREDIENT2E32821G6I1
PHOSPHORUSACTIVE INGREDIENT27YLU75U4W1
PULSATILLA VULGARISACTIVE INGREDIENTI76KB35JEV1
SILICON DIOXIDEACTIVE INGREDIENTETJ7Z6XBU41
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH139191
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 VULGARISACTIVE MOIETYI76KB35JEV1
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH139191
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43406-001743406-0017-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
OYSTER SHELL CALCIUM CARBONATE, CRUDE2E32821G6IACTIB
CHENOPODIUM AMBROSIOIDES4H5RSU087IACTIB
ANAMIRTA COCCULUS SEED810258W28UACTIB
CONIUM MACULATUM FLOWERING TOPQ28R5GF371ACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
PHOSPHORUS27YLU75U4WACTIB
PULSATILLA VULGARISI76KB35JEVACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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 HPOYSTER SHELL CALCIUM CARBONATE CRUDE, CHENOPODIUM AMBROSIOIDES, ANAMIRTA COCCULUS SEED, CONIUM MACULATUM FLOWERING TOP, STRYCHNOS NUX-VOMICA SEED, PHOSPHORUS, PULSATILLA VULGARIS, SILICON DIOXIDENatural Creations, Inc.9701096b-5efa-4acd-9227-339ecedfd6722025-12-10WarningsExact identifier
ndc (package): 43406-0017-1
ndc (product): 43406-0017
ndc11 (package): 43406001701
spl id: 05fb4634-169b-4384-9c7a-a5e3da911e1b
spl set id: 9701096b-5efa-4acd-9227-339ecedfd672

Reported adverse events (FAERS/openFDA)#

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