Minnerva II

LIDOCAINE, EPINEPHRINE TOPICAL HUMAN OTC DRUG

Minnerva II is an FDA drug label for the active ingredient LIDOCAINE, EPINEPHRINE manufactured by SofTap 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 20220505.

Generic name
LIDOCAINE, EPINEPHRINE
Manufacturer
SofTap Inc
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
82718-2210
Application
N/A
Label effective
20220505

About this product

Minnerva II is an FDA-registered drug product whose active ingredient is LIDOCAINE, EPINEPHRINE. It is labelled by SofTap Inc taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 82718-2210, label effective 20220505. 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, EPINEPHRINE are most often described in connection with: only temporarily, relieves pain, due cuts, scrapes abrasions. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

DRUG FACTS ACTIVE INGREDIENTS (per ml) PURPOSE Lidocaine USP - 4% topical anesthetic Epinephrine HCl - 0.4% vasoconstrictor FrontLabel

Indications & Usage

USES On adults over 18 only Temporarily relieves pain due to cuts, scrapes, or abrasions LabelPage1

Dosage & Administration

DIRECTIONS For external use only. Prior to application, a sensitivity test is advised. Before applying, cleanse the skin with an alcohol-free or acetone-free cleanser. Apply 1-2 cc to the desired area for up to 6 times per day. Discontinue use if allergic reaction occurs. Store in a cool dark place (up to 80 degrees F) or refrigerate. LabelPage3

Warnings

WARNINGS KEEP OUT OF REACH OF CHILDREN If swallowed seek medical help or contact Poison Control Center immediately.

Frequently asked questions

What is Minnerva II used for?
USES On adults over 18 only Temporarily relieves pain due to cuts, scrapes, or abrasions LabelPage1

Who makes Minnerva II?
SofTap Inc is the labeler of record for Minnerva II.

What form does Minnerva II 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 Minnerva II 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 Minnerva II 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.