Aspercreme Lidocaine XL

Aspercreme Lidocaine XL is an FDA-registered drug product whose active ingredient is LIDOCAINE. It is labelled by Lead Chemical Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 62168-0585, application 505G(a)(3), label effective 20260529. 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.

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.

Use for the temporary relief of pain

Directions • adults and children 12 years of age and older: • clean and dry affected area • remove backing from patch by firmly grasping both ends and gently pulling until backing separates in middle • carefully remove smaller portion of backing from patch and apply exposed portion of patch to affected area • once exposed portion of patch is positioned, carefully remove remaining backing to completely apply patch to affected area • apply to the affected area not more than 3 to 4 times daily • wash hands after applying or removing patch. Throw away the patch after folding sticky ends together. • children under 12 years of age: ask a doctor

Warnings For external use only Do not use • on wounds or on irritated or damaged skin • more than 1 patch on your body at a time or with other topical analgesics at the same time • with a heating pad When using this product • use only as directed • do not bandage tightly • avoid contact with eyes and mucous membranes • do not expose the area to local heat or to direct sunlight Stop use and ask a doctor if • condition worsens or symptoms persist for more than 7 days • symptoms clear up and occur again within a few days • redness is present or excessive skin irritation occurs • you experience severe burning pain, swelling, or blistering where the product was applied If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children and pets. Used patches may still contain the drug product that can produce serious adverse effects if ingested by children or pets. If swallowed, get medical help or contact a Poison Control Center right away.

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.

What is Aspercreme Lidocaine XL used for?
Use for the temporary relief of pain

Who makes Aspercreme Lidocaine XL?
Lead Chemical Co., Ltd. is the labeler of record for Aspercreme Lidocaine XL. 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 Aspercreme Lidocaine XL 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 Aspercreme Lidocaine XL 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 Aspercreme Lidocaine XL 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.