FDA Label for Arnica Scorodite
View Indications, Usage & Precautions
Arnica Scorodite 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: Amethyst (Nat. silicic acid anhydrate with traces of manganese and iron) 6X, Arnica 6X, Conchae (Oyster shells) 6X, Levisticum (Lovage) 6X, Natrium carb. (Sodium carbonate monohydrate) 6X, Orchis tub. decoct. (Orchid) 6X, Apatite (Nat. calcium fluorophosphate) 7X, Scorodite (Nat. ferric arsenate) 7X, Cerebellum (Bovine cerebellum) 8X
Inactive Ingredient
Inactive Ingredients: Sucrose, Lactose
Otc - Purpose
Use: Temporary relief of headache.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Warnings
Warnings: Contains sugar. Diabetics
and persons intolerant of sucrose (sugar): Consult a doctor before use. Do not use
if allergic to any ingredient. Contains traces of lactose. 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. Natural ingredients may cause color, scent and/or taste variation.
Otc - Questions
Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
www.urielpharmacy.com
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