FDA Label for Berberis Larix
View Indications, Usage & Precautions
Berberis Larix 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.
Purpose
Uses: Temporarily relieves symptoms of bladder irritation.
Dosage & Administration
Directions: Take at first sign of discomfort. Dissolve under tongue 3-4 times daily. Age 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: ask a doctor.
Indications & Usage
Uses: Temporarily relieves symptoms of bladder irritation.
Otc-Active Ingredient
Active Ingredients: Achillea (Yarrow) 3X, Berberis (Barberry) 3X, Equisetum (Common horsetail) 3X, Cantharis (Spanish fly) 6X, Apis (Honeybee) 8X, Pyrite (Nat. Iron disulfide) 8X, Resina laricis (Larch resin) 8X, Vesica urinaria (Bovine urinary bladder) 8X
Inactive Ingredient
Inactive Ingredient: Sucrose, Pyrite 8X, Vesica urinaria 8X.
Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Do Not Use Section
Warnings: Do not use if allergic to bee sting or any ingredient. Do not use if safety seal is broken or missing.
Ask Doctor Section
Urinary tract infection is a serious condition. Consult a doctor if you experience fever, pain in the kidney region, or changes in urine. Consult a doctor if you are diabetic or intolerant of sugar.
Pregnancy Or Breast Feeding Section
If you are pregnant or nursing, consult a doctor before use.
Questions Section
Questions? Uriel Pharmacy
866 642-2858 East Troy, WI 53120
www.urielpharmacy.com
NDC 48951-2043-2
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