Arth RX Topical Analgesic

METHYL NICOTINATE, CAPSAICIN TOPICAL HUMAN OTC DRUG

Arth RX Topical Analgesic is an FDA drug label for the active ingredient METHYL NICOTINATE, CAPSAICIN manufactured by HCD Sales 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 20231106.

Generic name
METHYL NICOTINATE, CAPSAICIN
Manufacturer
HCD Sales
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
76069-100
Application
M017
Label effective
20231106

About this product

Arth RX Topical Analgesic is an FDA-registered drug product whose active ingredient is METHYL NICOTINATE, CAPSAICIN. It is labelled by HCD Sales taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 76069-100, application M017, label effective 20231106. It is one of 2 FDA drug label records sharing the active ingredient METHYL NICOTINATE, CAPSAICIN. 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 METHYL NICOTINATE, CAPSAICIN are most often described in connection with: product avoid, apply wounds, damaged skin, bandage tightly. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredients Purpose Methyl nicotinate 0.5% External Analgesic Capsaicin 0.025 % External Analgesic

Indications & Usage

When Using This Product - Avoid contact with eyes - Do not apply to wounds or damaged skin - Do not bandage tightly

Dosage & Administration

Directions - Adults apply to affected area no more than 3-4 times daily - Children under 18 consult a physician - Apply to small area of the skin as test for sensitivity at least 60 minutes prior to applying to wide area.

Warnings

WARNINGS FOR EXTERNAL USE ONLY

More products with the same ingredient

METHYL NICOTINATE, CAPSAICIN

Arth Arrest

Key 2 Health, Inc. View label

How products containing METHYL NICOTINATE, CAPSAICIN compare

FDA lists 2 drug label records with METHYL NICOTINATE, CAPSAICIN 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 formProductsManufacturerProducts
— — HCD Sales 1
— — Key 2 Health, Inc. 1
— — — —
— — — —
— — — —

Frequently asked questions

What is Arth RX Topical Analgesic used for?
When Using This Product - Avoid contact with eyes - Do not apply to wounds or damaged skin - Do not bandage tightly

Who makes Arth RX Topical Analgesic?
HCD Sales is the labeler of record for Arth RX Topical Analgesic. 2 FDA label records share the active ingredient METHYL NICOTINATE, CAPSAICIN, 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 Arth RX Topical Analgesic 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 Arth RX Topical Analgesic 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 METHYL NICOTINATE, CAPSAICIN?
Yes. 2 FDA drug label records list METHYL NICOTINATE, CAPSAICIN 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 Arth RX Topical Analgesic 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.