myDerm MEDICAL NEW Soothing Hemorrhoidal

WITCH HAZEL PENYLEPHRINE LIDOCAINE TOPICAL HUMAN OTC DRUG

myDerm MEDICAL NEW Soothing Hemorrhoidal is an FDA drug label for the active ingredient WITCH HAZEL PENYLEPHRINE LIDOCAINE manufactured by Inspec Solutions 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 20260527.

Generic name
WITCH HAZEL PENYLEPHRINE LIDOCAINE
Manufacturer
Inspec Solutions
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
72667-287
Application
M015
Label effective
20260527

About this product

myDerm MEDICAL NEW Soothing Hemorrhoidal is an FDA-registered drug product whose active ingredient is WITCH HAZEL PENYLEPHRINE LIDOCAINE. It is labelled by Inspec Solutions taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 72667-287, application M015, label effective 20260527. 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 WITCH HAZEL PENYLEPHRINE LIDOCAINE are most often described in connection with: temporarily shrinks, hemorrhoidal tissue, reduces swelling, irritation helps, protect irritated, anorectal areas. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredients Purpose Witch Hazel Extract 50.00%.....................................................Anesthetic Lidocaine HCl 5.00%................................................................Anesthetic Phenylephrine Hydrochloride 0.25%................................Vasoconstrictor

Indications & Usage

Uses Temporarily shrinks hemorrhoidal tissue. • Temporarily reduces swelling associated with irritation • Helps protect irritated anorectal areas.

Dosage & Administration

Directions • Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. • Children under 2 years of age: Consult physician.

Warnings

Warnings For external use only. When using this product • avoid spraying in eyes. • contents under pressure. • do not puncture or incinerate. • do not store at temperature above 120° F. • do not exceed recommended daily dosage unless directed by doctor. • do not put this product into rectum by using fingers or any mechanical device or applicator. Ask a doctor or pharmacist before use if you have • heart disease, high blood pressure, thyroid disease, diabetes, difficulty in urination due to enlargement of prostate gland. • are presently taking a prescription drug for high blood pressure or depression. Stop use and ask doctor if • condition worsens, or if symptoms persist for more than 7 days, or clear up and reoccur again within a few days. If pregnant or breastfeeding, ask a healthcare professional before use.

Frequently asked questions

What is myDerm MEDICAL NEW Soothing Hemorrhoidal used for?
Uses Temporarily shrinks hemorrhoidal tissue. • Temporarily reduces swelling associated with irritation • Helps protect irritated anorectal areas.

Who makes myDerm MEDICAL NEW Soothing Hemorrhoidal?
Inspec Solutions is the labeler of record for myDerm MEDICAL NEW Soothing Hemorrhoidal.

What form does myDerm MEDICAL NEW Soothing Hemorrhoidal 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 myDerm MEDICAL NEW Soothing Hemorrhoidal 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 myDerm MEDICAL NEW Soothing Hemorrhoidal 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.