THE SOLU TION

LIDOCAINE HYDROCHLORIDE AND EPINEPHRINE HYDROCHLORIDE TOPICAL HUMAN OTC DRUG

THE SOLU TION is an FDA drug label for the active ingredient LIDOCAINE HYDROCHLORIDE AND EPINEPHRINE HYDROCHLORIDE manufactured by SCALP TECH INC 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 20260806.

Generic name
LIDOCAINE HYDROCHLORIDE AND EPINEPHRINE HYDROCHLORIDE
Manufacturer
SCALP TECH INC
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
82617-110
Application
M015
Label effective
20260806

About this product

THE SOLU TION is an FDA-registered drug product whose active ingredient is LIDOCAINE HYDROCHLORIDE AND EPINEPHRINE HYDROCHLORIDE. It is labelled by SCALP TECH INC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 82617-110, application M015, label effective 20260806. 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 HYDROCHLORIDE AND EPINEPHRINE HYDROCHLORIDE are most often described in connection with: temporary relief, anorectal itching, pain associated. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

ACTIVE INGREDIENTS LIDOCAINE HCL 5% EPINEPHRINE HCL .01%

Indications & Usage

USES FOR THE TEMPORARY RELIEF OF LOCAL AND ANORECTAL ITCHING, DISCOMFORT, AND PAIN ASSOCIATED WITH ANORECTAL DISORDERS OR ANORECTAL INFLAMMATION.

Dosage & Administration

DIRECTIONS ADULTS AND CHILDREN UNDER 12 YEARS OF AGE, CONSULT A DOCTOR. CLEAN THE AFFECTED AREA WITH MILD SOAP AND WATER. RINSE WELL OR PAT WITH APROPRIATE CLEANSING PAD GENTLY DRY BY PATTING OR BLOTTING WITH TOILET TISSUE OR A SOFT CLOTH BEFORE APPLYING THIS PRODUCT USE SPRAY PUMP TO APPLY EXTERNALLY TO THE AFFECTED AREA UP TO 4 TIMES DAILY DO NOT USE MORE OFTEN THAN DIRECTED

Warnings

WARNINGS FOR EXTERNAL USE ONLY. AVOID CONTACT WITH THE EYES.

Frequently asked questions

What is THE SOLU TION used for?
USES FOR THE TEMPORARY RELIEF OF LOCAL AND ANORECTAL ITCHING, DISCOMFORT, AND PAIN ASSOCIATED WITH ANORECTAL DISORDERS OR ANORECTAL INFLAMMATION.

Who makes THE SOLU TION?
SCALP TECH INC is the labeler of record for THE SOLU TION.

What form does THE SOLU TION 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 THE SOLU TION 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 THE SOLU TION 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.