Otc - Active Ingredient
Arnica montana 1X
The following Structured Product Label (SPL) was submitted to the FDA by Laboratoires Boiron for the product Arnicare (NDC 0220-9023). 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 otc - active ingredient, indications & usage, otc - do not use, dosage & administration, inactive ingredient, how supplied, otc - purpose, storage and handling, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Arnica montana 1X
Temporarily relives muscle pain and stiffness due to minor injuries, overexertion and falls.
Do not use if glued carton en flaps are open or if the tube seal is broken
Apply a thin layer of Arnicare Ointment to affected area and massage gently as soon as possible after minor injury. Repeat 3 times a day or as needed.
Alcohol, purified water, petrolatum USP
1 oz tube
Arnica montana 1X ...trauma, muscle pain and stiffness, swelling from injuries, discoloration from bruising.
Store at 68-77 O F (20-25 O C)
Questions, Comments?
www.arnicare.com
www.boironusa.com
1-800-BOIRON-1 (1-800-264-7661)
Distributed by Boiron Inc.
6 Campus Boulevard
Newtown Square, PA 19073-3267
Stop use and ask dotcor if condition persists for more than 3 days or worsens.
Keep out of reach of children
For external use only
Avoid contact with eyes and with open wounds.
If swallowed, get medical help or contact a Poison Control Center immediately
Arnicare Ointment Image
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