Arnica Nettle

FDA Drug Profile — Arnica Nettle

Arnica Nettle is listed in the FDA National Drug Code directory with 2 NDC codes, marketed under brand name including Arnica Nettle. Available dosage forms: gel, ointment.

Drug Details

Generic Name
Arnica Nettle
Brand Names
Arnica Nettle
Application Number
Sponsor
Uriel Pharmacy Inc.
NDC Codes
2
Dosage Forms
GEL, OINTMENT
Routes
TOPICAL
Active Ingredients
CALENDULA OFFICINALIS FLOWERING TOP, ARNICA MONTANA FLOWER, THUJA OCCIDENTALIS WHOLE, URTICA URENS, COMFREY ROOT, LYTTA VESICATORIA

Indications and Usage

Directions: FOR TOPICAL USE ONLY.

Warnings

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seal is broken or missing. FOR BURNS, SEEK MEDICAL ATTENTION IF NEEDED.