NEUROFLEX Topical Pain Relieving Liquid
NEUROFLEX Topical Pain Relieving Liquid is an FDA drug label for the active ingredient CAMPHOR (SYNTHETIC), MENTHOL manufactured by Almark Products 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 20231110.
- Generic name
- CAMPHOR (SYNTHETIC), MENTHOL
- Manufacturer
- Almark Products Inc
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 69876-1740
- Application
- M017
- Label effective
- 20231110
About this product
NEUROFLEX Topical Pain Relieving Liquid is an FDA-registered drug product whose active ingredient is CAMPHOR (SYNTHETIC), MENTHOL. It is labelled by Almark Products Inc taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 69876-1740, application M017, label effective 20231110. It is one of 4 FDA drug label records sharing the active ingredient CAMPHOR (SYNTHETIC), MENTHOL. 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 CAMPHOR (SYNTHETIC), MENTHOL are most often described in connection with: temporary relief, minor aches, pains muscles, joints arthritis, simple backaches, soreness strains, sprains bruises. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses For temporary relief of minor aches and pains of muscles and joints: • arthritis • simple backaches • soreness • strains • sprains • bruises
Dosage & Administration
Directions • Adults and children 2 years of age and older. Apply to affected areas not more than 3 to 4 times daily. No need to rub in. • Children under 2 years of age: Consult a physician.
Warnings
Warnings For External Use Only Flammable: Keep away from fire or flame. Do not use • on wounds • on damaged skin • on mucous membranes When using this product • avoid contact with eyes • do not bandage tightly • do not use a heating pad Stop use and ask a doctor if • condition worsens • symptoms persist for more than 7 days • symptoms clear up and occur again within a few days Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.
More products with the same ingredient
CAMPHOR (SYNTHETIC), MENTHOLRelieve and Relax Pain Relieving
View labelSMOOTH GATOR 60-second Pain Relief
View labelSMOOTH GATOR Foot and Leg Rub
View labelHow products containing CAMPHOR (SYNTHETIC), MENTHOL compare
FDA lists 4 drug label records with CAMPHOR (SYNTHETIC), MENTHOL 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 |
|---|---|---|---|
| — | — | Smooth Gator LLC | 2 |
| — | — | Almark Products Inc | 1 |
| — | — | MAC Innovations, LLC | 1 |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is NEUROFLEX Topical Pain Relieving Liquid used for?
Uses For temporary relief of minor aches and pains of muscles and joints: • arthritis • simple backaches • soreness • strains • sprains • bruises
Who makes NEUROFLEX Topical Pain Relieving Liquid?
Almark Products Inc is the labeler of record for NEUROFLEX Topical Pain Relieving Liquid. 4 FDA label records share the active ingredient CAMPHOR (SYNTHETIC), MENTHOL, 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 NEUROFLEX Topical Pain Relieving Liquid 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 NEUROFLEX Topical Pain Relieving Liquid 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 CAMPHOR (SYNTHETIC), MENTHOL?
Yes. 4 FDA drug label records list CAMPHOR (SYNTHETIC), MENTHOL 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 NEUROFLEX Topical Pain Relieving Liquid 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.