Arnica Gel

FDA Drug Profile — Arnica Gel 15 Arnica Montana 1X HPUS

Arnica Gel is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Arnica Gel 15 Arnica Montana 1X HPUS. Available dosage form: gel.

Drug Details

Generic Name
Arnica Gel
Brand Names
Arnica Gel 15 Arnica Montana 1X HPUS
Application Number
Sponsor
VITAMEDICA, INC.
NDC Codes
1
Dosage Forms
GEL
Routes
TOPICAL
Active Ingredients
HYPERICUM PERFORATUM, SYMPHYTUM OFFICINALE WHOLE, ARNICA MONTANA WHOLE, RHUS TYPHINA WHOLE, HAMAMELIS VIRGINIANA BARK, CALENDULA OFFICINALIS FLOWERING TOP, ARNICA MONTANA FLOWER, LEDUM PALUSTRE WHOLE, ACHILLEA MILLEFOLIUM FLOWER, BELLADONNA LEAF, BELLIS PERENNIS FLOWER, RUTA GRAVEOLENS WHOLE

Indications and Usage

USES: *Temporarily relieves these symptoms: • Bruising • Swelling • Pain • Stiff • Muscle Soreness *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Warnings

WARNINGS: For extrenal use only. Avoid contract with eyes and mucous membranes. Do not use on open wounds or broken skin Stop use or consult a physician if • A rash or irritation occurs • Symptoms persist for more than 7 days or worsen. Keep this and all medications out of reach of children. If sawllowed, seek medical attention or contact a Poison control center immediately.