Pain Relieving Gel-Patch

LIDOCAINE TOPICAL HUMAN OTC DRUG

Pain Relieving Gel-Patch is an FDA drug label for the active ingredient LIDOCAINE manufactured by Shanghai Chuangshi Medical Technology (Group) 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 20260629.

Generic name
LIDOCAINE
Manufacturer
Shanghai Chuangshi Medical Technology (Group) Co., Ltd.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
73557-177
Application
505G(a)(3)
Label effective
20260629

About this product

Pain Relieving Gel-Patch is an FDA-registered drug product whose active ingredient is LIDOCAINE. It is labelled by Shanghai Chuangshi Medical Technology (Group) Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 73557-177, application 505G(a)(3), label effective 20260629. It is one of 152 FDA drug label records sharing the active ingredient LIDOCAINE. 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 are most often described in connection with: temporary relief. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredient Lidocaine 4% ...... Purpose: Topical anesthetic

Indications & Usage

Uses For temporary relief of pain

Dosage & Administration

Directions Adult and Children 12 years of age and over: Clean and dry affected area Remove film from patch and apply to the skin (see illustration) Apply 1 patch at a time to affected area, not more than 3 to 4 times daily Remove patch from the skin after at most 8-hour application Children under 12 years of age: Consult a doctor

Warnings

Warnings For external use only

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How products containing LIDOCAINE compare

FDA lists 152 drug label records with LIDOCAINE 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
— — Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. 10
— — Shanghai Chuangshi Medical Technology (Group) Co., Ltd. 9
— — Proficient Rx LP 6
— — Bryant Ranch Prepack 5
— — Preferred Pharmaceuticals Inc. 5

Frequently asked questions

What is Pain Relieving Gel-Patch used for?
Uses For temporary relief of pain

Who makes Pain Relieving Gel-Patch?
Shanghai Chuangshi Medical Technology (Group) Co., Ltd. is the labeler of record for Pain Relieving Gel-Patch. 152 FDA label records share the active ingredient LIDOCAINE, 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 Pain Relieving Gel-Patch 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 Pain Relieving Gel-Patch 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?
Yes. 152 FDA drug label records list LIDOCAINE 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 Pain Relieving Gel-Patch 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.