Indications & Usage
Directions: FOR TOPICAL USE ONLY.
Quercus Essence
FDA Label NDC 48951-8119
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 Quercus Essence (NDC 48951-8119). 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
For compresses: Use 2 teaspoons per cup of lukewarm water. For full bath: Use 2-3 tablespoons.
Otc - Active Ingredient
Active Ingredient: Quercus e cort. 1X
Inactive Ingredient
Inactive Ingredients: Distilled water, 20% Organic cane alcohol
Otc - Purpose
Use: Temporary relief of skin rash.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Warnings
Warnings: FOR EXTERNAL USE ONLY. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seal is broken or missing.
Otc - Questions
Questions? Call 866.642.2858 Made with care by Uriel, East Troy, WI 53120 www.urielpharmacy.com
* Please review the disclaimer below.
