Active Ingredients:
(HPUS) Arnica Montana 30C
Arnica Relief Tablet
FDA Label NDC 61727-111
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Homeocare Laboratories for the product Arnica Relief (NDC 61727-111). 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 active ingredients:, purpose:, indications & usage:, warnings:, keep out of reach of children., inactive ingredients:, dosage & administration:, arnica montana 30c, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose:
Helps reduce bruising, swelling and pain associated with injuries, trauma, surgical procedures and arthritis.
Indications & Usage:
Helps reduce bruising, swelling, and pain associated with injuries, trauma, surgical procedures, and arthritis.
Warnings:
If symptoms persist or worsen, or if nursing, consult a doctor. Keep out of reach of children. Do not use if cap seal is broken or missing.
Keep Out Of Reach Of Children.
Keep out of reach of children.
Inactive Ingredients:
Sucrose/lactose.
Dosage & Administration:
Turn tube upside down, twist cap to break seal & release pellets. Using clear cap, place 3 pellets to dissolve under your tongue 3 times a day or as needed. Take apart from food or drinks. To preserve purity avoid touching pellets with fingers.
* Please review the disclaimer below.
