Deep Numbing Cream

Deep Numbing Cream is an FDA-registered drug product whose active ingredient is MENTHOL. It is labelled by YITONGBADA (SHENZHEN) INTERNATIONAL TRADE CO., LTD taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 83364-023, application M017, label effective 20260413. It is one of 193 FDA drug label records sharing the active ingredient MENTHOL. 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 are most often described in connection with: temporary relief, localized pain, itching discomfort, minor skin, product avoid, recommended daily, dosage unless, directed doctor. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses ■ For the temporary relief of localized pain, itching, or discomfort from minor skin irritations. When using this product ■ Avoid contact with eyes ■ Do not exceed the recommended daily dosage unless directed by a doctor. ■ Do not put this product into the rectum by using fingers or any mechanical device or applicator. Stop use and ask a doctor if ■ Condition worsens or does not improve within 7 days. ■ An allergic reaction occurs to ingredients in this product. ■ Redness, irritation, swelling, pain, or other symptoms develop or increase. ■ Symptoms clear up and occur again within a few days. Keep out of reach of children. In case of accidental ingestion, seek medical advice immediately or contact a Poison Control Center right away. If pregnant or breastfeeding, ask a health professional before use.

Directions ■ When practical, cleanse the affected area with mild soap and warm water, then rinse thoroughly. ■ Gently dry by patting or blotting with toilet tissue or a soft cloth before applying. ■ Adults and children 12 years 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

FDA lists 193 drug label records with MENTHOL 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 Deep Numbing Cream used for?
Uses ■ For the temporary relief of localized pain, itching, or discomfort from minor skin irritations. When using this product ■ Avoid contact with eyes ■ Do not exceed the recommended daily dosage unless directed by a doctor. ■ Do not put this product into the rectum by using fingers or any mechanical device or applicator. Stop use and ask a doctor if ■ Condition worsens or does not improve …

Who makes Deep Numbing Cream?
YITONGBADA (SHENZHEN) INTERNATIONAL TRADE CO., LTD is the labeler of record for Deep Numbing Cream. 193 FDA label records share the active ingredient MENTHOL, 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 Deep 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 Deep 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?
Yes. 193 FDA drug label records list MENTHOL 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 Deep 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.