Velloryn EXTRA STRENGTH NEUROPATHY
Velloryn EXTRA STRENGTH NEUROPATHY is an FDA drug label for the active ingredient VELLORYN EXTRA STRENGTH NEUROPATHY manufactured by GUANGZHOU YUSONG FINE CHEMICLS 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 20260617.
- Generic name
- VELLORYN EXTRA STRENGTH NEUROPATHY
- Manufacturer
- GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 84558-020
- Application
- M017
- Label effective
- 20260617
About this product
Velloryn EXTRA STRENGTH NEUROPATHY is an FDA-registered drug product whose active ingredient is VELLORYN EXTRA STRENGTH NEUROPATHY. 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 84558-020, application M017, label effective 20260617. 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 VELLORYN EXTRA STRENGTH NEUROPATHY are most often described in connection with: temporarily relieves, minor muscle, joint pain, including tingling, foot discomfort. 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 minor muscle and joint pain, including tingling, burning, and foot discomfort
Dosage & Administration
Directions adults and children 2 years and older: apply to affected area up to 3-4 times daily massage gently until absorbed children under 2 years: ask a doctor
Warnings
Warnings For external use only
Frequently asked questions
What is Velloryn EXTRA STRENGTH NEUROPATHY used for?
Use Temporarily relieves minor muscle and joint pain, including tingling, burning, and foot discomfort
Who makes Velloryn EXTRA STRENGTH NEUROPATHY?
GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd is the labeler of record for Velloryn EXTRA STRENGTH NEUROPATHY.
What form does Velloryn EXTRA STRENGTH NEUROPATHY 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 Velloryn EXTRA STRENGTH NEUROPATHY 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.
Has Velloryn EXTRA STRENGTH NEUROPATHY 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.