Indications & Usage
Directions: FOR ORAL USE ONLY.
Arsenicum 6/12/30 Special Order
FDA Label NDC 48951-1291
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 Arsenicum 6/12/30 Special Order (NDC 48951-1291). 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
Use up to every hour. Ages 2 and older: 1-2 sprays. Under age 2: Consult a doctor.
Otc - Active Ingredient
Active Ingredients: Arsenicum album (White arsenic) 6X/12X/30X
Inactive Ingredient
Inactive Ingredients: Distilled water, 30% Organic cane alcohol, Lactose
Otc - Purpose
Uses: 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. Contains traces of lactose. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seals on box are broken or missing.
Otc - Questions
Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
www.urielpharmacy.com
Package Label.Principal Display Panel
Arsenicum61230sospray (Arsenicum61230sospray)
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