Menthol Pain Relieving Gel
Menthol Pain Relieving Gel is an FDA drug label for the active ingredient PAIN RELIEVING GEL manufactured by NeilMed Pharmaceuticals Inc 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 20260507.
- Generic name
- PAIN RELIEVING GEL
- Manufacturer
- NeilMed Pharmaceuticals Inc
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 13709-357
- Application
- M014
- Label effective
- 20260507
About this product
Menthol Pain Relieving Gel is an FDA-registered drug product whose active ingredient is PAIN RELIEVING GEL. It is labelled by NeilMed Pharmaceuticals Inc taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 13709-357, application M014, label effective 20260507. 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 PAIN RELIEVING GEL are most often described in connection with: indications cooling, pain relieving, muscle aches, simple backache. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Indications Cooling, Pain relieving gel for muscle aches arthiritis pain simple backache Indications
Dosage & Administration
Dosage and Administration Menthol 2 % Therapeutic Greaseless Net Wt- 8 FL OZ (227 g) Dosage and Administration
Warnings
Warnings For External Use Only. Avoid Contact with eyes. Warnings
Recall and safety notices
1 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.
| Recall | Product | Firm | Class | Status | Reported |
|---|---|---|---|---|---|
| D-0569-2024 | SinuFrin Decongestant (oxymetazoline HCl) Nasal Solution Nasal Decongestant, Decongestant Relief for up to 12 Hours, 12 Hour Relief, 0.5 fl oz (15 ml) bottle, Manufactured by NeilMed Pharmaceuticals Inc, 602 Aviation Blvd, Santa Rosa, CA 95403 877-477-8633; NDC 13709-325-01; UPC 7 05928 09001 9. | Neilmed Pharmaceuticals Inc | Class III | Ongoing | 20240703 |
Frequently asked questions
What is Menthol Pain Relieving Gel used for?
Indications Cooling, Pain relieving gel for muscle aches arthiritis pain simple backache Indications
Who makes Menthol Pain Relieving Gel?
NeilMed Pharmaceuticals Inc is the labeler of record for Menthol Pain Relieving Gel.
What form does Menthol Pain Relieving Gel 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 Menthol Pain Relieving Gel 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 Menthol Pain Relieving Gel been recalled?
1 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.
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.