Indications & Usage
Directions: ONLY FOR USE AS A NASAL SPRAY.
Viscum Quercus 1%
FDA Label NDC 48951-9322
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Uriel Pharmacy Inc. for the product Viscum Quercus 1% (NDC 48951-9322). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding indications & usage, dosage & administration, otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, warnings, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Dosage & Administration
Ages 12 and older: 2-3 sprays. Ages 2-11: 1-2 sprays. Under age 2: Consult a doctor.
Otc - Active Ingredient
Active Ingredient: Viscum album
(Quercus) 1X
Inactive Ingredient
Inactive Ingredients: Distilled water, Sea
salt, Grapefruit seed extract
Otc - Purpose
Use: Temporary relief of headache.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Warnings
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seals on box are broken or missing.
SHAKE WELL BEFORE USE.
REFRIGERATE AFTER OPENING.
USE WITHIN 30 DAYS OF OPENING.
Otc - Questions
Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
www.urielpharmacy.com
Package Label.Principal Display Panel
Viscumquercus1nasalspray (Viscumquercus1nasalspray)
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