Purpose
Uses: Temporary relieves symptoms of sore throat and mouth inflammation.
Purple Coneflower
FDA Label NDC 48951-8318
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 Purple Coneflower (NDC 48951-8318). 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, warnings, 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: Take up to every 1-2 hours as needed. Ages 12 and older: 2-3 sprays. Ages 2-11: 1-2 sprays. Under age 2: Ask a doctor.
Otc-Active Ingredient
Active Ingredients: Calendula 1X, Echinacea (Purple coneflower) 1X, Eucalyptus 1X, Salvia (Sage) 1X, Gingiva (Bovine gums) 8X, Tonsilla (Bovine tonsil) 8X, Vaucheria (Fresh water algae) 8X, Argentum nitricum (Silver nitrate) 21X, Atropa belladonna (Nightshade) 21X, Quartz (Rock crystal) 21X
Inactive Ingredient
Inactive Ingredients: Organic cane alcohol, Water, Eucalyptus oil, Gingiva, Tonsilla, Vaucheria.
Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Warnings
Do not use if allergic to any ingredient. Do not use if safety seal is broken or missing.
Ask Doctor Section
Consult a doctor if symptoms worsen or persist.
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
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Purpleconeflowerspray (Purpleconeflowerspray)
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