ORLASKIN HYDROGEL EYE MASK

ALLANTOIN TOPICAL HUMAN OTC DRUG

ORLASKIN HYDROGEL EYE MASK is an FDA drug label for the active ingredient ALLANTOIN manufactured by Guangzhou Yapheon Health Industry 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 20260626.

Generic name
ALLANTOIN
Manufacturer
Guangzhou Yapheon Health Industry Co., Ltd.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
87582-007
Application
M016
Label effective
20260626

About this product

ORLASKIN HYDROGEL EYE MASK is an FDA-registered drug product whose active ingredient is ALLANTOIN. It is labelled by Guangzhou Yapheon Health Industry Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87582-007, application M016, label effective 20260626. It is one of 9 FDA drug label records sharing the active ingredient ALLANTOIN. 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 ALLANTOIN are most often described in connection with: apply one, patch clean, dry skin, gently massage, remaining serum, skinuse daily. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

ActiveIngredient.Allantoin 0.5% PurposeSkin Protectant

Indications & Usage

apply one patch to clean, dry skin under each eyeleave on for 15-20 minutesremove and gently massage remaining serum into skinuse daily or as needed

Dosage & Administration

avoid contact with eyes Stop use and ask a doctor if condition worsens symptoms last more than 7 days symptoms clear up and occur again within a few days

Warnings

WARNINGS For external use only

More products with the same ingredient

ALLANTOIN

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DeFlame

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Drs. pharmacy Scar Cream

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Mederma Advanced Scar

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Mederma Advanced Scar

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How products containing ALLANTOIN compare

FDA lists 9 drug label records with ALLANTOIN 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
— — L. Perrigo Company 2
— — Galderma Laboratories, L.P. 1
— — Guangzhou Yapheon Health Industry Co., Ltd. 1
— — Noon Aesthetics M.R. Ltd 1
— — OL PHARMA TECH, LLC Drs PHARMACY 1

Frequently asked questions

What is ORLASKIN HYDROGEL EYE MASK used for?
apply one patch to clean, dry skin under each eyeleave on for 15-20 minutesremove and gently massage remaining serum into skinuse daily or as needed

Who makes ORLASKIN HYDROGEL EYE MASK?
Guangzhou Yapheon Health Industry Co., Ltd. is the labeler of record for ORLASKIN HYDROGEL EYE MASK. 9 FDA label records share the active ingredient ALLANTOIN, 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 ORLASKIN HYDROGEL EYE MASK 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 ORLASKIN HYDROGEL EYE MASK 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 ALLANTOIN?
Yes. 9 FDA drug label records list ALLANTOIN 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 ORLASKIN HYDROGEL EYE MASK 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.