Welmate Numbing Relief

LIDOCAINE 5% TOPICAL HUMAN OTC DRUG

Welmate Numbing Relief is an FDA drug label for the active ingredient LIDOCAINE 5% manufactured by YYBA Corp 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 20260708.

Generic name
LIDOCAINE 5%
Manufacturer
YYBA Corp
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
73581-920
Application
M015
Label effective
20260708

About this product

Welmate Numbing Relief is an FDA-registered drug product whose active ingredient is LIDOCAINE 5%. It is labelled by YYBA Corp taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 73581-920, application M015, label effective 20260708. It is one of 13 FDA drug label records sharing the active ingredient LIDOCAINE 5%. 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 LIDOCAINE 5% are most often described in connection with: local itching, pain associated, anorectal disorders. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Lidocaine 5%

Indications & Usage

For the local itching and pain associated with anorectal disorders or inflammation.

Dosage & Administration

When practical, cleanse the affected area with mild soap and warm water, Rinse thoroughly and gently pat dry. Spray affected area. Wash hands after applying. Adults and children 2 years of age and older, apply externally to the affected area up to 6 times a day. Children under 12 years of age: consult a doctor.

Warnings

For external use only. Flammable-- Keep away from fire or flame. When using this product avoid contact with eyes, do not exceed recommended dosage unless directed by a doctor, do not put this product into the rectum by using fingers or any mechanical device or applicator, contents under pressure. Do not puncture or incinerate. Do not store at temperatures above 120F. Stop use and ask a doctor if rectal bleeding occurs, condition worsens or does not improve within 7 days, allergic reaction occurs to ingredients in this product, symptom being treated does not subside or if redness, irritation, swelling, pain or other symptoms develop or increase. i

More products with the same ingredient

LIDOCAINE 5%

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How products containing LIDOCAINE 5% compare

FDA lists 13 drug label records with LIDOCAINE 5% 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
— — EveryMarket Inc 5
— — A-S Medication Solutions 1
— — Alera Skin Care Products Inc. 1
— — Injecta Medcial LLC 1
— — Jiangxi Yudexi Pharmaceutical Co., LTD 1

Frequently asked questions

What is Welmate Numbing Relief used for?
For the local itching and pain associated with anorectal disorders or inflammation.

Who makes Welmate Numbing Relief?
YYBA Corp is the labeler of record for Welmate Numbing Relief. 13 FDA label records share the active ingredient LIDOCAINE 5%, 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 Welmate Numbing 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 Welmate Numbing 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 LIDOCAINE 5%?
Yes. 13 FDA drug label records list LIDOCAINE 5% 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 Welmate Numbing 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.