SIERQ Numbing

SIERQ Numbing is an FDA-registered drug product whose active ingredient is MENTHOL. It is labelled by Putian Licheng District Zhijiancheng Trading Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87152-006, application M017, label effective 20260816. 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: ask doctorcondition, improve within, daysallergic reaction, occurs ingredients, product symptom, subside redness. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Stop Use and Ask a DoctorCondition worsens or does not improve within 7 daysAllergic reaction occurs to ingredients in this product.Symptom being treated does not subside or if redness, irritation

DirectionsAdults and children 2 years of age and older:Apply to affected area not more than 3 to 4 times dailyChildren under 2 years of age: Do not use, consult a doctor

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 • Do not use in large quantities, particularly over raw surfaces or blistered areas • Avoid contact with eyes. If this happens, rinse thoroughly with wate

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 SIERQ Numbing used for?
Stop Use and Ask a DoctorCondition worsens or does not improve within 7 daysAllergic reaction occurs to ingredients in this product.Symptom being treated does not subside or if redness, irritation

Who makes SIERQ Numbing?
Putian Licheng District Zhijiancheng Trading Co., Ltd. is the labeler of record for SIERQ Numbing. 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 SIERQ 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 SIERQ 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 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 SIERQ 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.