Otc - Purpose
Use: Temporary relief of headache.
Sabal Populus Liquid
FDA Label NDC 48951-8161
8 label sections · Submitted to the FDA by Uriel Pharmacy Inc. · 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 Sabal Populus (NDC 48951-8161). 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 otc - purpose, indications & usage, dosage & administration, warnings, otc - keep out of reach of children, otc - active ingredient, inactive ingredient, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Indications & Usage
FOR ORAL USE ONLY
Dosage & Administration
Directions: Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow. Follow inside instructions to open ampule.
Warnings
Warnings:
NOT FOR INJECTION
Do not use if allergic to any ingredient. Consult a physician if symptoms worsen. If pregnant or nursing, consult a physician before use.
Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Otc - Active Ingredient
Active Ingredients: Berberis (Barberry) 3X, Populus trem (Aspen) 3X, Sabal serr. (Dwarf palm) 3X, Solidago (Goldenrod) 3X, Thuja (American arborvitae) 6X, Magnesite (Nat. magnesium carbonate) 12X
Inactive Ingredient
Inactive Ingredients: Water, Salt
Prepared using rhythmical processes.
Otc - Questions
Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 shopuriel.com Lot:
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