Lidocaine Phenylephrine
Lidocaine Phenylephrine is an FDA drug label for the active ingredient LIDOCAINE PHENYLEPHRINE manufactured by YYBA CORP administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260901.
- Generic name
- LIDOCAINE PHENYLEPHRINE
- Manufacturer
- YYBA CORP
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 73581-910
- Application
- M015
- Label effective
- 20260901
About this product
Lidocaine Phenylephrine is an FDA-registered drug product whose active ingredient is LIDOCAINE PHENYLEPHRINE. It is labelled by YYBA CORP taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 73581-910, application M015, label effective 20260901. 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.
What it is used for
Across FDA labelling, products containing LIDOCAINE PHENYLEPHRINE are most often described in connection with: temporarily reduces, swelling associated, irritated hemorrhoidal, anorectal disorders. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Use temporarily reduces swelling associated with irritated hemorrhoidal tissue and other anorectal disorders
Dosage & Administration
Directions when practical, cleanse the affected area with mild soap and warm water rinse thoroughly and gently pat dry spray affected area wash hands after applying replace cap after use Adults and children 12 years or older: apply externally to affected area not more than 4 times daily Children under 12 years of age: do not use, ask a doctor
Warnings
Warnings For external use only.
Frequently asked questions
What is Lidocaine Phenylephrine used for?
Use temporarily reduces swelling associated with irritated hemorrhoidal tissue and other anorectal disorders
Who makes Lidocaine Phenylephrine?
YYBA CORP is the labeler of record for Lidocaine Phenylephrine.
What form does Lidocaine Phenylephrine 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 Lidocaine Phenylephrine 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.
Has Lidocaine Phenylephrine 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.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.