Dosage & Administration
Directions: FOR ORAL USE.
Cichorium Oxalis Liquid
FDA Label NDC 48951-3091
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 Cichorium Oxalis (NDC 48951-3091). 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 dosage & administration, otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, warnings, otc - questions, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
Active Ingredients: Cichorium e pl. tota 3X, Oxalis e pl. tota 3X, Carbo Betulae 6X, Pancreas 6X, Barium citricum 10X, Ferrum sidereum 20X
Inactive Ingredient
Inactive Ingredients: Water, Salt
Otc - Purpose
Use: Temporary relief of headache.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Warnings
Warnings: 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.
Otc - Questions
Questions? Call 866.642.2858 Made by Uriel, East Troy, WI 53120 www.urielpharmacy.com
* Please review the disclaimer below.
