Dizzy Formula

Manufacturer
Nutritional Specialties, Inc.
Effective date
2026-03-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:38:15

Label at a glance#

ProductDizzy Formula
Active ingredientARNICA MONTANA WHOLE, CENTELLA ASIATICA FLOWERING TOP, AMBERGRIS, SILVER NITRATE, ANAMIRTA COCCULUS SEED, CONIUM MACULATUM FLOWERING TOP, CANIS LUPUS FAMILIARIS MILK, THERIDION CURASSAVICUM
Label structure9 sections

Indications and uses

For temporary relief of •dizziness, •light headedness, and •sensations of motion or spinning.† †Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Dosage and administration

• Adults: 2 to 3 sprays orally, three times daily. • Children under twelve one half adult dosage. • Do not take within 15 minutes of consuming food, beverage or brushing teeth. 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 spray) Ambra Grisea 12X, Argentum Nitricum 12X, Arnica Montana 3X, Cocculus Indicus 12X, Conium Maculatum 12X, Hydrocotyle Asiatica 3X, Lac Caninum 12X, Theridion 18X.

PURPOSE:

OTC - PURPOSE SECTION

Ambra Grisea – Dizziness, and Sensations of Motion or Spinning,† Argentum Nitricum – Dizziness, Light Headedness, and Sensations of Motion or Spinning,† Arnica Montana – Dizziness, Light Headedness, and Sensations of Motion or Spinning,† Cocculus Indicus – Dizziness, Light Headedness, and Sensations of Motion or Spinning,† Conium Maculatum – Dizziness, and Light Headedness,† Hydrocotyle Asiatica – Dizziness, and Sensations of Motion or Spinning,† Lac Caninum – Dizziness, and Sensations of Motion or Spinning,† Theridion – Dizziness, Light Headedness, and Sensations of Motion or Spinning†

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

USES:

INDICATIONS & USAGE SECTION

For temporary relief of •dizziness, •light headedness, and •sensations of motion or spinning.†

†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.

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

If condition worsens, seek medical attention.

KEEP OUT OF REACH OF CHILDREN

Do not use if tamper evident seal is broken or missing.

Store in a cool place after opening

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

• Adults: 2 to 3 sprays orally, three times daily.

• Children under twelve one half adult dosage.

• Do not take within 15 minutes of consuming food, beverage or brushing teeth.

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

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Alcohol USP 20%, Purified Water USP.

QUESTIONS:

OTC - QUESTIONS SECTION

MANUFACTURED EXCLUSIVELY FOR

NUTRITIONAL SPECIALTIES, INC.

PO BOX 97227

PITTSBURG, PA 15229

www.phpltd.com

1-800-245-1313

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Professional

Health Products

HOMEOPATHIC

NDC 83027-0001-1

DIZZY FORMULA

2 FL. OZ. (60 ml)

DIZZY FORMULADIZZY FORMULA

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130649818031150GTIN-13: 0649818031150
EAN-13: 0649818031150
GTIN-12: 649818031150
UPC-A: 649818031150
GTIN storage (14 digits): 00649818031150
NSPC0008 Dizzy Formula 2oz 12-23-25.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83027-0001-1Dizzy Formula60 mL in 1 BOTTLE, SPRAYSPRAY602

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
83027-000183027-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
Dizzy FormulaARNICA MONTANA, HYDROCOTYLE ASIATICA, AMBRA GRISEA, ARGENTUM NITRICUM, COCCULUS INDICUS, CONIUM MACULATUM, LAC CANINUM, THERIDIONNutritional Specialties, Inc.aaccfd13-6559-4976-90d1-aa3b4a4a79db2026-03-31WarningsExact identifier
ndc (package): 83027-0001-1
ndc (product): 83027-0001
ndc11 (package): 83027000101
spl id: bc927253-1a40-44ad-8ef5-46240f498cf0
spl set id: aaccfd13-6559-4976-90d1-aa3b4a4a79db

Reported adverse events (FAERS/openFDA)#

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