Arnica Bruise Cream

Arnica Bruise Cream is an FDA-registered drug product whose active ingredient is ARNICA MONTANA. It is labelled by Beautivity LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85398-005, label effective 20260629. It is one of 23 FDA drug label records sharing the active ingredient ARNICA MONTANA. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing ARNICA MONTANA are most often described in connection with: helps reduce, appearance bruises, skin discoloration, soothes discomfort, caused minor. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Helps reduce the appearance of bruises, swelling, and skin discoloration. Soothes discomfort caused by minor injuries

Apply a thin layer of Arnica Bruise Cream to affected area and massage gently as soon as possible after minor injury. Repeat 3 times a day or as needed. If heat or ice is applied, wait 5 minutes before applying Arnica Bruise Cream

For external use only. if you are allergic to Arnica Montana or any inactive ingredients in this product. Avoid contact with eyes, mucous membranes, wounds, damaged or irritated skin. Use only as directed. Do not tightly wrap or bandage the treated area. Do not apply heat or ice to the treated area immediately before or after use. Stop use and ask a doctor if: Condition persists for more than 3 days or worsens. Symptoms clear up and occur again within a few days If swallowed, get medical help or contact a Poison Control Center right away.

FDA lists 23 drug label records with ARNICA MONTANA as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is Arnica Bruise Cream used for?
Helps reduce the appearance of bruises, swelling, and skin discoloration. Soothes discomfort caused by minor injuries

Who makes Arnica Bruise Cream?
Beautivity LLC is the labeler of record for Arnica Bruise Cream. 23 FDA label records share the active ingredient ARNICA MONTANA, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Arnica Bruise Cream come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Arnica Bruise Cream prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing ARNICA MONTANA?
Yes. 23 FDA drug label records list ARNICA MONTANA as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Arnica Bruise Cream been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.