PUTRIZEN

UNDECYLENIC ACID, TOLNAFTATE TOPICAL HUMAN OTC DRUG

PUTRIZEN is an FDA drug label for the active ingredient UNDECYLENIC ACID, TOLNAFTATE manufactured by Guangzhou Lianbiquan Biological Technology co., Ltd 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 20260525.

Generic name
UNDECYLENIC ACID, TOLNAFTATE
Manufacturer
Guangzhou Lianbiquan Biological Technology co., Ltd
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
87724-5118
Application
M005
Label effective
20260525

About this product

PUTRIZEN is an FDA-registered drug product whose active ingredient is UNDECYLENIC ACID, TOLNAFTATE. It is labelled by Guangzhou Lianbiquan Biological Technology co., Ltd taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87724-5118, application M005, label effective 20260525. It is one of 3 FDA drug label records sharing the active ingredient UNDECYLENIC ACID, TOLNAFTATE. 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 UNDECYLENIC ACID, TOLNAFTATE are most often described in connection with: athlete foot, tinea pedis, corporis relieves, itching burning. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredient(s) Undecylenic Acid 25% Tolnaftate 1%

Indications & Usage

Uses cures most athlete's foot (tinea pedis) and ringworm (tinea corporis) ​ relieves itching, burning. cracking, and scaling which accompany these conditions

Dosage & Administration

Directions clean the affected area and dry thoroughly apply a thin layer to the affected area twice daily (morning and night) or as directed by a doctor for athlete's foot pay special attention to spaces between the toes, wearwell-fitting, venulated shoes, and change shoes and socks at least once dally for best results, use daily for at least 4 weeks

Warnings

Warnings For external use only Flammable: keep away from heat and flame Do not use On children under 2 years of age unless directed by a doctor When using this product avoid contact with eyes use only as directed do not use on broken or irritated skin unless directed by a doctor do not bandage tightly Stop use and ask a doctor if irritation occurs or gets worse there is no improvement within 4 weeks

More products with the same ingredient

UNDECYLENIC ACID, TOLNAFTATE

DrAny NAIL FUNGUS TREATMENT

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GUANGZHOU SAWEILAN IMPORT & EXPORT TRADING CO., LTD View label

How products containing UNDECYLENIC ACID, TOLNAFTATE compare

FDA lists 3 drug label records with UNDECYLENIC ACID, TOLNAFTATE as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

Dosage formProductsManufacturerProducts
— — GUANGZHOU SAWEILAN IMPORT & EXPORT TRADING CO., LTD 1
— — Guangzhou Lianbiquan Biological Technology co., Ltd 1
— — Hong Kong Juxin Negosyo Kag Komersyo Co., Limited 1
— — — —
— — — —

Frequently asked questions

What is PUTRIZEN used for?
Uses cures most athlete's foot (tinea pedis) and ringworm (tinea corporis) ​ relieves itching, burning. cracking, and scaling which accompany these conditions

Who makes PUTRIZEN?
Guangzhou Lianbiquan Biological Technology co., Ltd is the labeler of record for PUTRIZEN. 3 FDA label records share the active ingredient UNDECYLENIC ACID, TOLNAFTATE, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does PUTRIZEN 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 PUTRIZEN 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.

Are there other products containing UNDECYLENIC ACID, TOLNAFTATE?
Yes. 3 FDA drug label records list UNDECYLENIC ACID, TOLNAFTATE as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has PUTRIZEN 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.