DERMFREE PAIN RELIEF
DERMFREE PAIN RELIEF is an FDA drug label for the active ingredient ARNICA MONTANA HPUS 7% PAIN RELIEF manufactured by Jiangxi Yudexi Pharmaceutical Co., LTD 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 20260724.
- Generic name
- ARNICA MONTANA HPUS 7% PAIN RELIEF
- Manufacturer
- Jiangxi Yudexi Pharmaceutical Co., LTD
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 85248-145
- Application
- M017
- Label effective
- 20260724
About this product
DERMFREE PAIN RELIEF is an FDA-registered drug product whose active ingredient is ARNICA MONTANA HPUS 7% PAIN RELIEF. It is labelled by Jiangxi Yudexi Pharmaceutical Co., LTD taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85248-145, application M017, label effective 20260724. It is one of 2 FDA drug label records sharing the active ingredient ARNICA MONTANA HPUS 7% PAIN RELIEF. 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.
What it is used for
Across FDA labelling, products containing ARNICA MONTANA HPUS 7% PAIN RELIEF are most often described in connection with: temporarily relieves, muscle pain, stiffness due, minor injuries, overexertion falls, reduces symptoms, swelling discoloration. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Use temporarily relieves muscle pain and stiffness due to: ■Minor injuries ■Overexertion ■falls reduces symptoms of bruising such as: ■Pain■Swelling ■Discoloration
Dosage & Administration
Directions Apply a thin layer of the cream to the affected area as soon as possible after minor injury. Repeat 3 times daily or as needed.If heat or ice is applied, wait 5 minutes before applying the cream.
Warnings
Warnings For external use only
More products with the same ingredient
ARNICA MONTANA HPUS 7% PAIN RELIEFHow products containing ARNICA MONTANA HPUS 7% PAIN RELIEF compare
FDA lists 2 drug label records with ARNICA MONTANA HPUS 7% PAIN RELIEF 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.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Jiangxi Yudexi Pharmaceutical Co., LTD | 2 |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is DERMFREE PAIN RELIEF used for?
Use temporarily relieves muscle pain and stiffness due to: ■Minor injuries ■Overexertion ■falls reduces symptoms of bruising such as: ■Pain■Swelling ■Discoloration
Who makes DERMFREE PAIN RELIEF?
Jiangxi Yudexi Pharmaceutical Co., LTD is the labeler of record for DERMFREE PAIN RELIEF. 2 FDA label records share the active ingredient ARNICA MONTANA HPUS 7% PAIN RELIEF, 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 DERMFREE PAIN RELIEF 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 DERMFREE PAIN RELIEF 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 HPUS 7% PAIN RELIEF?
Yes. 2 FDA drug label records list ARNICA MONTANA HPUS 7% PAIN RELIEF 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 DERMFREE PAIN RELIEF 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.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.