Allergy

Manufacturer
Zorex International | OHM Pharma, Inc
Effective date
2018-12-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:20:55

Label at a glance#

ProductAllergy
Active ingredientONION, AMBROSIA ARTEMISIIFOLIA WHOLE, ACTIVATED CHARCOAL, EUPHRASIA STRICTA, STRYCHNOS NUX-VOMICA SEED, PHOSPHORUS, PULSATILLA VULGARIS WHOLE, SULFUR, SOLIDAGO VIRGAUREA FLOWERING TOP
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS (*HPUS): equal amounts of: Allium Cepa 30C, Ambrosia 30C, Arsenicum Alb 30C, Carbo Veg 30C, Euphrasia 30C, Nux Vom 30C, Phosphorus 30C, Pulsatilla 30C, Sulphur 30C, Solidago 30C

INDICATIONS & USAGE SECTION

USES: Temporarily relieves hay fever, coryza, itching and burning eyes, coughing and/or other symptoms associated with hay fever and allergies.**

OTC - PURPOSE SECTION

USES: Temporarily relieves hay fever, coryza, itching and burning eyes, coughing and/or other symptoms associated with hay fever and allergies.**

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: Ethyl Alcohol USP, Purified Water

OTC - QUESTIONS SECTION

QUESTIONS & COMMENTS?

Zorex International LTD. / Lowell, MI 49331 / 800-679-3027

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:81825-0007-1

Allergy

HOMEOPATHIC

1 fl oz (30mL) / 20% Alcohol

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81825-0007-1Allergy30 mL in 1 BOTTLE, DROPPERLIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81825-0007ALLERGY (ALLIUM CEPA, AMBROSIA, ARSENICUM ALB, CARBO VEG, EUPHRASIA, NUX VOM, PHOSPHORUS, PULSATILLA, SULPHUR, SOLIDAGO) LIQUID [ZOREX INTERNATIONAL]1Current NDC, 1 package rows20230420_4718c012-b90d-4d7a-a97c-1abec1fd3834.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81825-000781825-0007-1

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

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
AllergyALLIUM CEPA, AMBROSIA, ARSENICUM ALB, CARBO VEG, EUPHRASIA, NUX VOM, PHOSPHORUS, PULSATILLA, SULPHUR, SOLIDAGOZorex International4718c012-b90d-4d7a-a97c-1abec1fd38342018-12-21WarningsExact identifier
ndc (package): 81825-0007-1
ndc (product): 81825-0007
ndc11 (package): 81825000701
spl id: dda1ff79-ce5d-47c0-99e6-0b77f3defed7
spl set id: 4718c012-b90d-4d7a-a97c-1abec1fd3834

Reported adverse events (FAERS/openFDA)#

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