PUTRIZEN ARNICA BRUISE RELIEF Cream

PUTRIZEN ARNICA BRUISE RELIEF Cream is an FDA-registered drug product whose active ingredient is PUTRIZEN ARNICA BRUISE RELIEF CREAM. It is labelled by GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 84558-030, application 505G(a)(3), label effective 20260816. It is one of 2 FDA drug label records sharing the active ingredient PUTRIZEN ARNICA BRUISE RELIEF CREAM. 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 PUTRIZEN ARNICA BRUISE RELIEF CREAM are most often described in connection with: temporary relief, pain swelling, discoloration due, minor bruising, muscle overexertion, skin discomfort. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Use For the temporary relief of pain, swelling, and discoloration due to ▪ minor bruising ▪ muscle overexertion ▪ or skin discomfort.

Directions Apply a thin layer to the affected area 2-3 times daily. Gently massage into fragile or delicate skin areas. If heat or ice is applied, wait 5 minutes before applying Arnica Bruise Cream.

Warnings For external use only.

FDA lists 2 drug label records with PUTRIZEN ARNICA BRUISE RELIEF CREAM 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 PUTRIZEN ARNICA BRUISE RELIEF Cream used for?
Use For the temporary relief of pain, swelling, and discoloration due to ▪ minor bruising ▪ muscle overexertion ▪ or skin discomfort.

Who makes PUTRIZEN ARNICA BRUISE RELIEF Cream?
GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd is the labeler of record for PUTRIZEN ARNICA BRUISE RELIEF Cream. 2 FDA label records share the active ingredient PUTRIZEN ARNICA BRUISE RELIEF CREAM, 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 PUTRIZEN ARNICA BRUISE RELIEF 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 PUTRIZEN ARNICA BRUISE RELIEF 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 PUTRIZEN ARNICA BRUISE RELIEF CREAM?
Yes. 2 FDA drug label records list PUTRIZEN ARNICA BRUISE RELIEF CREAM 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 PUTRIZEN ARNICA BRUISE RELIEF 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.