Purpose
Uses: Temporarily relieves symptoms of heavy menstrual flow.
Tormentilla Cochlearia
FDA Label NDC 48951-9281
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 Tormentilla Cochlearia (NDC 48951-9281). 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 purpose, dosage & administration, otc-active ingredient, inactive ingredient, keep out of reach of children, do not use if allergic to any ingredient. do not use if safety seal is broken or missing., ask doctor section, pregnancy or breast feeding section, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Dosage & Administration
Directions: Dissolve under tongue every 2 hours during menstrual periods with heavy bleeding. Age 12 and older: 10 pellets. Under age 12: ask a doctor.
Otc-Active Ingredient
Active Ingredients: Cochlearia (Common scurvy grass) 3X, Tormentilla (Bloodwort) 3X, Stibium met. (Antimony) 6X
Inactive Ingredient
Inactive Ingredient: Sucrose.
Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Do Not Use If Allergic To Any Ingredient. Do Not Use If Safety Seal Is Broken Or Missing.
Ask Doctor Section
Heavy menstrual flow may indicate a serious condition. Consult a doctor if symptoms persist, 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 48951-9017-2
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