Kevo-Prophen

JUNIPER TAR TOPICAL HUMAN OTC DRUG

Kevo-Prophen is an FDA drug label for the active ingredient JUNIPER TAR manufactured by Faeve, LLC 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 20260420.

Generic name
JUNIPER TAR
Manufacturer
Faeve, LLC
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
87607-001
Application
M017
Label effective
20260420

About this product

Kevo-Prophen is an FDA-registered drug product whose active ingredient is JUNIPER TAR. It is labelled by Faeve, LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87607-001, application M017, label effective 20260420. 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 JUNIPER TAR are most often described in connection with: temporary relief. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredient Juniperus Oxycedrus (Juniper Tar Oil) 1%

Indications & Usage

Use For the temporary relief of pain

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: do not use, consult a physician.

Warnings

Warnings For External Use Only Use only as directed Read and follow directions on label Avoid contact with eyes and muscous membranes. If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician. If pregnant or breast feeding, ask a physician before use. Keep out of reach of children If swallowed, get medical help or contact Poison Control Center right away. DO NOT USE on puncture wounds on cut, irritated, or open skin.

Frequently asked questions

What is Kevo-Prophen used for?
Use For the temporary relief of pain

Who makes Kevo-Prophen?
Faeve, LLC is the labeler of record for Kevo-Prophen.

What form does Kevo-Prophen 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 Kevo-Prophen 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 Kevo-Prophen 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.