Subleef NUMBING

LIDOCAINE4% NUMBING TOPICAL HUMAN OTC DRUG

Subleef NUMBING is an FDA drug label for the active ingredient LIDOCAINE4% NUMBING manufactured by Jiangxi Yudexi Pharmaceutical 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 20260720.

Generic name
LIDOCAINE4% NUMBING
Manufacturer
Jiangxi Yudexi Pharmaceutical Co., LTD
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
85248-052
Application
M017
Label effective
20260720

About this product

Subleef NUMBING is an FDA-registered drug product whose active ingredient is LIDOCAINE4% NUMBING. It is labelled by Jiangxi Yudexi Pharmaceutical Co., LTD taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85248-052, application M017, label effective 20260720. It is one of 4 FDA drug label records sharing the active ingredient LIDOCAINE4% NUMBING. 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 LIDOCAINE4% NUMBING are most often described in connection with: temporary relief, itching associated, minor burns, sunburn insect, skin irritations. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredient Lidocaine 4%

Indications & Usage

Use For the temporary relief of pain and itching associated with minor burns, sunburn, insect bites and minor skin irritations

Dosage & Administration

Directions Adults and children 2 years of age and older.Apply to affected area not more than 3 to 4 times daily.Children under 2 years of age: Do not use, consult a doctor

Warnings

Warnings ·For external use only. ·If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor

More products with the same ingredient

LIDOCAINE4% NUMBING

ANIXIKE Numbing

Jiangxi Yudexi Pharmaceutical Co., LTD View label

ANIXIKE Numbing

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DERMFREE NUMBING

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How products containing LIDOCAINE4% NUMBING compare

FDA lists 4 drug label records with LIDOCAINE4% NUMBING 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
— — Jiangxi Yudexi Pharmaceutical Co., LTD 4
— — — —
— — — —
— — — —
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Frequently asked questions

What is Subleef NUMBING used for?
Use For the temporary relief of pain and itching associated with minor burns, sunburn, insect bites and minor skin irritations

Who makes Subleef NUMBING?
Jiangxi Yudexi Pharmaceutical Co., LTD is the labeler of record for Subleef NUMBING. 4 FDA label records share the active ingredient LIDOCAINE4% NUMBING, 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 Subleef NUMBING 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 Subleef NUMBING 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 LIDOCAINE4% NUMBING?
Yes. 4 FDA drug label records list LIDOCAINE4% NUMBING 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 Subleef NUMBING 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.