Walgreens Arnica
Walgreens Arnica is an FDA drug label for the active ingredient ARNICA MONTANA 7% manufactured by Walgreens administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20221130.
Generic: ARNICA MONTANA 7%
Manufacturer: Walgreens
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 0363-3034
Application:
Effective: 20221130
Active Ingredients: Arnica montana 1 X HPUS 7%
Indications & Usage
Temporarily relieves muscle pain and stiffness due to minor injuries, overexertion and falls reduces pain, swelling and discoloration from bruises.
Dosage & Administration
Directions: adults and children over 12 years: Apply to affected area and massage until thoroughly absorbed into skin. Repeat 3 times a day or as needed. Children 12 years or younger : ask a doctor
Contraindications
Not available.
Warnings
For external use only Do not use if you are allergic to Arnica montana or to any of this product's inactive ingredients. Extremely Flammable do not use near heat or flame or while smoking avoid long term storage above 104°F (40°C) do not puncture or incinerate. Contents under pressure do not store at temperatures above 120°F (49°C) When using this product Use only as directed Avoid spraying on face Avoid inhalation of spray Do not bandage or apply local heat (such as heating pads) or a medicated patch to area of use Stop use and ask a doctor if irritation develops condition persist for more than 3 days or worsens If pregnant or breast feeding , ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a poison Control Center right away.
Adverse Reactions
Not available.
More from same ingredient
No related products.