FDA Label for Cinnabar Dandelion
View Indications, Usage & Precautions
Cinnabar Dandelion Product Label
The following document was submitted to the FDA by the labeler of this product Uriel Pharmacy Inc.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Indications & Usage
Directions: FOR ORAL USE ONLY.
Dosage & Administration
Dissolve pellets under the tongue 3-4 times daily. Ages 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: Consult
a doctor.
Otc - Active Ingredient
Active Ingredients: Taraxacum (Dandelion) 2X, Agropyrum (Couch grass) 3X, Pyrite (Nat. Iron disulfide) 3X, Kali carb. e cin. Fagi (Potassium carbonate from beech wood ash) 10X, Cinnabaris (Nat. mercuric sulfide) 20X
Inactive Ingredient
Inactive Ingredients: Organic sucrose, Lactose
Otc - Purpose
Uses: Temporarily relieves symptoms of cold, flu and sore throat.
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. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. Contains lactose. 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 seal is broken or missing.
Otc - Questions
Questions? Call 866.642.2858
Made by Uriel, East Troy, WI 53120
www.urielpharmacy.com
* Please review the disclaimer below.