FDA Label for Allergy
View Indications, Usage & Precautions
Allergy Product Label
The following document was submitted to the FDA by the labeler of this product Zorex International. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
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
USES: Temporarily relieves hay fever, coryza, itching and burning eyes, coughing and/or other symptoms associated with hay fever and allergies.**
Otc - Purpose
USES: Temporarily relieves hay fever, coryza, itching and burning eyes, coughing and/or other symptoms associated with hay fever and allergies.**
Dosage & Administration
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
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
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
INACTIVE INGREDIENTS: Ethyl Alcohol USP, Purified Water
Otc - Questions
QUESTIONS & COMMENTS?
Zorex International LTD. / Lowell, MI 49331 / 800-679-3027
References
*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
* Please review the disclaimer below.