Indications & Usage
Directions: FOR ORAL USE.
Arnica Echinacea
FDA Label NDC 48951-1141
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 Arnica Echinacea (NDC 48951-1141). 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 indications & usage, dosage & administration, otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, warnings, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Dosage & Administration
Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.
Otc - Active Ingredient
Active Ingredients: Bellis per. ex herba 5X, Echinacea e pl. tota 5X, Hamamelis e fol. 5X, Hypericum ex herba 5X, Achillea ex herba 6X, Aconitum e tub. 6X, Arnica e pl. tota 6X, Atropa belladonna ex herba 6X, Calendula ex herba 6X, Chamomilla e pl. tota 6X, Hepar sulfuris 9X, Mercurius solubilis 9X, Symphytum ex herba 9X
Inactive Ingredient
Inactive Ingredients: Water, Salt
Otc - Purpose
Uses: Temporary relief of bruises, sprains and minor cuts.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Warnings
Warnings: Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use.
Otc - Questions
Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
www.urielpharmacy.com
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