SERYNTH HEMORRHOID

SERYNTH HEMORRHOID is an FDA-registered drug product whose active ingredient is LIDOCAINE 4% PHENYLEPHRINE HCL 0.25% HEMORRHOID. It is labelled by Jiangxi Yudexi Pharmaceutical Co., LTD taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85248-155, application M017, label effective 20260724. It is one of 4 FDA drug label records sharing the active ingredient LIDOCAINE 4% PHENYLEPHRINE HCL 0.25% HEMORRHOID. 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 4% PHENYLEPHRINE HCL 0.25% HEMORRHOID are most often described in connection with: temporarily shrink, hemorrhoidal tissue, relieving pain, soreness burning, itching anddiscomfort. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Use Temporarily shrink hemorrhoidal tissue, relieving pain,soreness, burning, itching, anddiscomfort associated with hemorrhoids.

Directions Children under 12 years of age consult your pediatrician. Adults: apply to affected area up to 3 times daily.Clean affected area with mild soap and warm water, rinse thoroughly, and then gently dry (patting or blotting) with tissue or soft cloth before use. To use dispensing cap, attach it to tube, lubricate well then gently insert part way into anus and squeeze tube to deliver medication. Thoroughly cleanse dispensing cap after use with mild soap and warm water and rinse thoroughly.

Warnings For external use only, including the skin aroundthe anal canal

FDA lists 4 drug label records with LIDOCAINE 4% PHENYLEPHRINE HCL 0.25% HEMORRHOID 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 SERYNTH HEMORRHOID used for?
Use Temporarily shrink hemorrhoidal tissue, relieving pain,soreness, burning, itching, anddiscomfort associated with hemorrhoids.

Who makes SERYNTH HEMORRHOID?
Jiangxi Yudexi Pharmaceutical Co., LTD is the labeler of record for SERYNTH HEMORRHOID. 4 FDA label records share the active ingredient LIDOCAINE 4% PHENYLEPHRINE HCL 0.25% HEMORRHOID, 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 SERYNTH HEMORRHOID 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 SERYNTH HEMORRHOID 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 4% PHENYLEPHRINE HCL 0.25% HEMORRHOID?
Yes. 4 FDA drug label records list LIDOCAINE 4% PHENYLEPHRINE HCL 0.25% HEMORRHOID 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 SERYNTH HEMORRHOID 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.