PUTRIZEN 40 UREA

GLYCERIN TOPICAL HUMAN OTC DRUG

PUTRIZEN 40 UREA is an FDA drug label for the active ingredient GLYCERIN manufactured by Shantou Ximonth Biotechnology 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 20260601.

Generic name
GLYCERIN
Manufacturer
Shantou Ximonth Biotechnology Co., Ltd.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
84989-025
Application
M016
Label effective
20260601

About this product

PUTRIZEN 40 UREA is an FDA-registered drug product whose active ingredient is GLYCERIN. It is labelled by Shantou Ximonth Biotechnology Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 84989-025, application M016, label effective 20260601. It is one of 37 FDA drug label records sharing the active ingredient GLYCERIN. 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 GLYCERIN are most often described in connection with: feet heels, elbows knees, rough areas, wash hands. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

BUTYROSPERMUM PARKII (SHEA) BUTTER、SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL、MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL

Indications & Usage

Use on feet, heels, elbows, knees, or other rough areas. Wash hands after use.

Dosage & Administration

Use on feet, heels, elbows, knees, or other rough areas. Wash hands after use.

Warnings

For external use only. Avoid contact with eyes. Do not use on broken, irritated, or sensitive skin. Discontinue use if irritation or rash occurs. Keep out of reach of children. Do not swallow.

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How products containing GLYCERIN compare

FDA lists 37 drug label records with GLYCERIN 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
— — Shantou Ximonth Biotechnology Co., Ltd. 12
— — Guangzhou Houkea Biotechnology Co., Ltd. 4
— — Shantou Eelhoe Daily Chemical Technology Co., Ltd. 4
— — Shantou Ouhoe Technology Co., Ltd. 3
— — Beijing Jingfeng Pharmaceutical (Shandong) Co., Ltd 2

Frequently asked questions

What is PUTRIZEN 40 UREA used for?
Use on feet, heels, elbows, knees, or other rough areas. Wash hands after use.

Who makes PUTRIZEN 40 UREA?
Shantou Ximonth Biotechnology Co., Ltd. is the labeler of record for PUTRIZEN 40 UREA. 37 FDA label records share the active ingredient GLYCERIN, 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 40 UREA 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 40 UREA 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 GLYCERIN?
Yes. 37 FDA drug label records list GLYCERIN 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 40 UREA 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.