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Magnet Eye Sheet Mask .5 mg/100g Patch, 430 g — NDC 84753-0039-02 package photo

Magnet Eye Sheet Mask .5 mg/100g Patch, 430 g

by Guangdong Bisutang Biotechnology Co., LTD · 430 g in 1 BOX (84753-039-02)
NDC 84753-0039-02
🏷️ FDA NDC (as labeled) 84753-039-02 billing pads the product segment with a zero
This package
Contains430 g Pack sizes3 compare ↓
Also comes in: 1 patch 84753-0039-03 200 g 84753-0039-01
OTC On market Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

🆔 Identity & classification

FDA NDC (as labeled) 84753-039-02
Product NDC 84753-039
11-digit billing NDC 84753003902
RxCUI 1441556
UNII 344S277G0Z
Application # M016
SPL Set ID 4a0a84d4-4024-5ea7-e063-6394a90a2b6c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-02-05
Route TOPICAL
Dosage form PATCH
Substance ALLANTOIN
Why two NDCs? The FDA registers this code as 84753-039-02 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 84753-0039-02. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏭 Manufacturer & labeler

LabelerGuangdong Bisutang Biotechnology Co., LTD
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code84753
First marketedFeb 2026
Product typeHuman Otc Drug
Portfolio5 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

🧪 What is this product?

This is an over-the-counter topical patch marketed under FDA's monograph rules for skin care products. The patch contains allantoin, an ingredient commonly used in skin products to help soothe and moisturize the skin around the eyes. The product is designed to be applied directly to the eye area as a sheet mask or patch. Allantoin is typically included in cosmetic and skin care formulations for its moisturizing and skin-conditioning properties.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

💊 What it looks like

Color white
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII TR046Y3K1G
    A liquid alcohol derived from petroleum or plant sources. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • UNII 6MW60CB71P
    A stabilized form of vitamin C used as an antioxidant in medicines. It prevents other ingredients from breaking down or discoloring during storage.
  • UNII 8Z5ZAL5H3V
    A synthetic polymer made from acrylate compounds. It acts as a thickener and stabilizer in topical formulations, helping create the right texture and prevent separation of ingredients.
  • UNII 05545M0E3M
    A plant extract from agave leaves used as a natural sweetener and flavoring agent in medicines. It helps improve taste and may serve as a binder or thickening ingredient in liquid or semi-solid formulations.
  • UNII ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • UNII WN5C16297P
    A live beneficial bacterium commonly found in the human gut. It serves as an active probiotic ingredient that may support digestive health and immune function.
  • UNII 3XUS85K0RA
    Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
  • UNII 3G6A5W338E
    Caffeine is a natural stimulant compound commonly extracted from coffee beans and tea leaves. In medicines, it serves as an active booster in pain relievers and cold products to enhance alertness and improve the effectiveness of other ingredients.
  • UNII P0M7O4Y7YD
    A plant extract from calendula flowers, traditionally used in formulations. It typically serves as a botanical ingredient that may provide color, fragrance, or skin-conditioning properties to topical products.
  • UNII UPY805K99W
    A synthetic compound derived from caprylic acid that works as a preservative and antimicrobial agent to help prevent bacterial and fungal growth in the medicine.
  • UNII 6810070TYD
    Centella asiatica leaf is a plant extract used in medicines as a skin-conditioning agent and natural ingredient. It may help soften or soothe the product's texture and is included for its traditional botanical properties in topical or oral formulations.
  • UNII 4370DF050B
    Ceramide NP is a waxy, lipid-based substance that mimics natural skin oils. It's used in topical formulations as an emollient and skin-conditioning agent to help soften, smooth, and protect the skin barrier.
  • UNII J7IHY79BKY
    A plant extract from glasswort, a coastal herb. It's used in formulations as a humectant to help retain moisture and may serve as a skin-conditioning agent in topical products.
  • UNII 7E6SK9QDT8
    Cyclodextrins are ring-shaped sugar molecules derived from starch. They're used in medicines as solubilizers to help poorly dissolving drugs dissolve better, and sometimes as binders or stabilizers.
  • UNII QH92QT9LWR
    A synthetic fragrance mixture used to improve the taste or smell of the medicine. It helps mask bitter or unpleasant flavors and odors, making the medication more pleasant to take.
  • UNII 6YSS42VSEV
    Fructose is a natural sugar derived from fruits and plants. It's used in medicines as a sweetener and filler to improve taste and add bulk to tablets or syrups.
  • UNII NNE56F2N14
    A synthetic compound derived from glycerin and polyethylene glycol. It acts as an emulsifier and solubilizer to help mix water and oil-based ingredients and keep them blended throughout the product's shelf life.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII TM2TZD4G4A
    A plant-derived oily substance used as an emulsifier and solubilizer in medicines. It helps blend water and oil-based ingredients together and improves how the body absorbs certain active drugs.
  • UNII 151Z7P1317
    Hexyldecanol is a waxy alcohol derived from natural oils. It acts as an emollient and viscosity agent in topical formulations, helping create smooth texture and improve product spreadability on skin.
  • UNII H1109Z9J4N
    A natural emulsifier derived from soybean oil. It helps mix oil and water-based ingredients together, ensuring even distribution of active ingredients throughout the medicine.
  • UNII G1L3HT4CMH
    A synthetic compound used in medicines as a preservative and antimicrobial agent. It helps prevent bacterial and fungal growth, extending the product's shelf life.
  • UNII 5307V7XW8I
    A beneficial bacterium added to certain medicines and supplements. It acts as a probiotic ingredient, helping maintain or restore healthy gut bacteria balance in formulations designed for digestive wellness.
  • UNII XJ6S9RV06F
    Maltose is a simple sugar made from grain starches. It works as a sweetener and filler in medicines to improve taste and add bulk to tablets and powders.
  • UNII VIF565UC2G
    Tea tree oil is an essential oil extracted from the leaves of the Australian tea tree plant. In medicines, it typically serves as a flavoring agent, fragrance, or antimicrobial component in topical formulations.
  • UNII N8F53B3R4R
    A synthetic humectant and solvent derived from propane. It draws and holds moisture in the formulation, helping keep the medicine stable and improving texture or flow in liquid and semi-solid products.
  • UNII 25X51I8RD4
    Niacinamide is a form of vitamin B3, a water-soluble nutrient. In medicines, it may be added as a nutritional supplement or to support skin health, though its primary role here is as an active ingredient rather than a traditional inactive filler.
  • UNII Q41S464P1R
    A synthetic peptide (short protein-like molecule) used in skincare and cosmetic formulations as an active conditioning ingredient to help improve skin texture and appearance. It may function as a humectant or skin-conditioning agent in topical products.
  • UNII RV743D216M
    A synthetic peptide derived from fatty acids and amino acids. It functions as a skin-conditioning agent and emollient in topical formulations, helping soften and smooth the product texture while supporting skin hydration.
  • UNII 7YC686GQ8F
    A synthetic oily substance made from castor oil. It works as a solubilizer and emulsifier to help mix oily and water-based ingredients together in the medicine.
  • UNII 50C1307PZG
    Pentylene glycol is a humectant and preservative helper derived from petroleum or plant sources. It draws moisture into the product and helps prevent bacterial growth, keeping medicines stable during storage.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII WZH3C48M4T
    Potassium hydroxide is a strong alkaline chemical used in medicines to adjust and maintain the pH level of liquid formulations, helping keep the product stable and the active ingredients effective.
  • UNII 724GKU717M
    Jojoba oil is a natural liquid wax extracted from jojoba plant seeds. It's used in medicines as an emollient and lubricant to soften and smooth the product, and sometimes as a carrier or penetration enhancer.
  • UNII YSE9PPT4TH
    Hyaluronate sodium is a natural carbohydrate that holds moisture. It's used in medicines as a lubricant, thickener, and moisture-retaining agent to improve texture and delivery of the active ingredient.
  • UNII 4938BNS0GU
    A fungal extract from tremella fuciformis, a jelly-like mushroom. It acts as a thickener, emulsifier, and skin-conditioning agent in topical formulations to improve texture and moisture retention.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
  • UNII TTV12P4NEE
    Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.
  • UNII 44FQ49X6UN
    A polysaccharide (complex carbohydrate) derived from yeast cell walls. In medicines, it acts as a binder to hold tablet ingredients together and may help with tablet structure and stability.

39 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesWATER GLYCERIN BUTYLENE GLYCOL GLYCERETH-26 NIACINAMIDE PENTYLENE GLYCOL FRUCTOSE LACTOBACILLUS METHYLPROPANEDIOL SODIUM HYALURONATE MALTOSE HYDROXYACETOPHENONE XANTHAN GUM CYCLODEXTRIN CAFFEINE HEXYLDECANOL AGAVE TEQUILANA LEAF 3-O-ETHYL ASCORBIC ACID ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) CAPRYLHYDROXAMIC ACID 1,2-HEXANEDIOL POTASSIUM HYDROXIDE TREMELLA FUCIFORMIS WHOLE PEG-40 HYDROGENATED CASTOR OIL BIFIDOBACTERIUM BIFIDUM HYDROGENATED SOYBEAN LECITHIN CERAMIDE NP YEAST.BETA.-D-GLUCAN GLYCERYL CAPRYLATE FRAGRANCE CRITHMUM MARITIMUM MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL CENTELLA ASIATICA LEAF CALENDULA OFFICINALIS FLOWER ALOE BARBADENSIS LEAF PHENOXYETHANOL PALMITOYL TRIPEPTIDE-1 PALMITOYL TETRAPEPTIDE-7

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer eachPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Try another pack size: 1 patch 200 g
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Magnet Eye Sheet Mask .5 mg/100gthis 84753-0039-02 Guangdong 430 g — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

⏳ Availability & generic status

🏛️
2026
On the market since
Feb 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
84753-0039-01 200 g in 1 BOX (84753-039-01) 2026-02-05 Active
84753-0039-02 You're viewing this 430 g in 1 BOX (84753-039-02) 2026-02-05 Active
84753-0039-03 15 g in 1 PATCH (84753-039-03) 2026-02-24 Active

You're viewing the largest of 3 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 84753-0039-02?
NDC 84753-0039-02 contains 430 g — 430 g in 1 box.
What is the difference between NDC 84753-0039-02 and NDC 84753-0039-03?
Both are Magnet Eye Sheet Mask .5 mg/100g Patch — the drug itself is identical. NDC 84753-0039-02 is the 430 g package, while NDC 84753-0039-03 is the 1 patch package.
What NDC number is used to bill for this package of Magnet Eye Sheet Mask .5 mg/100g Patch?
Bill NDC 84753-0039-02 — the 11-digit billing format is 84753003902. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 84753-039-02, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 84753-0039-02, written without dashes as 84753003902. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 84753-0039-02, the first segment (84753) is the labeler code FDA assigned to Guangdong Bisutang Biotechnology Co., LTD; the middle segment (0039) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Guangdong Bisutang Biotechnology Co., LTD. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 2 other package presentations of this same product, including 1 patch (84753-0039-03), 200 g (84753-0039-01). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Guangdong Bisutang Biotechnology Co., LTD is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.

📄 FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 72 words ▾

How to Apply:Our formula is designed to be gentle for the delicate eye area.Gently place the mask on the entire eye contour area, ensuring asmooth fit. The unique cut-out design helps protect your eyes. Ifany essence gets into the eyes, simply rinse with water. After removing the mask, gently massage anyremaining essence into the skin. For a fresh finish,we recommend lightly rinsing the eye area withwater and proceeding with your regular skincareroutine.

⏱️ Dosage and Administration 17 words ▾

For best results, apply for 10-15 minutes. This product isdesigned for single-use only. Discard promptly after oneapplication.

⚠️ Warnings 29 words ▾

Warning: For external use only. If you have specific skin or health concerns, please consult a dermatologist or healthcare professional before use. Keep out of reach of children section.

🧪 Active Ingredient 1 words ▾

ALLANTOIN------0.5%

🧪 Inactive Ingredients 83 words ▾

WATER GLYCERIN BUTYLENE GLYCOL GLYCERETH-26 NIACINAMIDE PENTYLENE GLYCOL FRUCTOSE LACTOBACILLUS METHYLPROPANEDIOL SODIUM HYALURONATE MALTOSE HYDROXYACETOPHENONE XANTHAN GUM CYCLODEXTRIN CAFFEINE HEXYLDECANOL AGAVE TEQUILANA LEAF 3-O-ETHYL ASCORBIC ACID ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) CAPRYLHYDROXAMIC ACID 1,2-HEXANEDIOL POTASSIUM HYDROXIDE TREMELLA FUCIFORMIS WHOLE PEG-40 HYDROGENATED CASTOR OIL BIFIDOBACTERIUM BIFIDUM HYDROGENATED SOYBEAN LECITHIN CERAMIDE NP YEAST .BETA.-D-GLUCAN GLYCERYL CAPRYLATE FRAGRANCE CRITHMUM MARITIMUM MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL CENTELLA ASIATICA LEAF CALENDULA OFFICINALIS FLOWER ALOE BARBADENSIS LEAF PHENOXYETHANOL PALMITOYL TRIPEPTIDE-1 PALMITOYL TETRAPEPTIDE-7

🎯 Purpose 19 words ▾

Smooth Fine Lines Weaken Dark Circles Relieve Puffines Skin Brightening Firm the skin Enhance skin elasticity Firm the skin

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 84753-0038-01 · Guangdong 84753-0040-01 · Guangdong →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.