FDA Label for Antimonite Belladonna
View Indications, Usage & Precautions
Antimonite Belladonna 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
Take 3-4 times daily. Ages 12 and older: 1/8 teaspoon. Ages 2-11: 1/16 teaspoon. Under age 2: Consult a doctor.
Otc - Active Ingredient
Active Ingredients: Antimonite (Nat. antimony trisulfide) 3X, Atropa belladonna (Nightshade) 4X, Chamomilla (Chamomile) 4X, Bismutum subnitricum (Bismuth) 6X
Inactive Ingredient
Inactive Ingredient: Lactose
Otc - Purpose
Use: Temporary relief of upset stomach.
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. Do not use if allergic to any ingredient. Contains 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.
Otc - Questions
Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 www.urielpharmacy.com
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