Aemerry Numbing Cream

Aemerry Numbing Cream is an FDA-registered drug product whose active ingredient is MENTHOL 5%. It is labelled by Da Capo Prima LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87615-002, application M017, label effective 20260420. It is one of 6 FDA drug label records sharing the active ingredient MENTHOL 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.

Across FDA labelling, products containing MENTHOL 5% are most often described in connection with: yearsof age, consult doctor, product cleanthe, affected area, mild soap, andwarm water, rinsethoroughly pat, soft cloth. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Children(under 12 yearsof age):consult a doctor. Adults: before applying this product, cleanthe affected area with mild soap andwarm water and rinsethoroughly.Pat drythe area with a soft cloth or tissue. Apply up to 3 times a day.

Temporarily relieves local and anorectal discomfort associated with the anorectal disorder or swelling.

For external use only Do not use this product if youare allergic to lidocaine. in case of accidental overdose, seek immedidate medical help or contact the Poison Control Center. seal is broken or missing. When using this product donot exceed the recommended daily dosage unless directed by a doctor. Certain sensitive individualsmayhave an allergic reaction to some of the ingredients of this product. do not put this cream into the rectum using your fingers, applicators, or any medical devices. Stop use and ask a doctor if the symptom being treated does not improve, or ifredness,irritation, swelling, pain, or other symptoms appear or worsen. Seek medical help right away. In case of accidental ingestion, seek medical help right away.

FDA lists 6 drug label records with MENTHOL 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.

What is Aemerry Numbing Cream used for?
Children(under 12 yearsof age):consult a doctor. Adults: before applying this product, cleanthe affected area with mild soap andwarm water and rinsethoroughly.Pat drythe area with a soft cloth or tissue. Apply up to 3 times a day.

Who makes Aemerry Numbing Cream?
Da Capo Prima LLC is the labeler of record for Aemerry Numbing Cream. 6 FDA label records share the active ingredient MENTHOL 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 Aemerry Numbing Cream 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 Aemerry Numbing Cream 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 MENTHOL 5%?
Yes. 6 FDA drug label records list MENTHOL 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 Aemerry Numbing Cream 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.