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Arthcal TURMERIC NIGHT WRAPPING MASK 5 g/100mL; 5 g/100mL; 2000-5000 MW) Gel, 75 mL

by Beijing JUNGE Technology Co., Ltd. · 75 mL in 1 CONTAINER (85212-0033-1)
NDC 85212-0033-01
🏷️ FDA NDC (as labeled) 85212-0033-1 billing pads the package segment with a zero
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) 85212-0033-1
Product NDC 85212-0033
11-digit billing NDC 85212003301
UNII W5488JUO8U
Application # 505G(a)(3)
SPL Set ID 33fbb589-8267-6c8d-e063-6394a90a0922
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-01-01
Route EXTRACORPOREAL
Dosage form GEL
Substance CURCUMA LONGA WHOLE; HYDROLYSED BOVINE COLLAGEN (ENZYMATIC; 2000-5000 MW)
Why two NDCs? The FDA registers this code as 85212-0033-1 — a 5-4-1 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 package segment → 85212-0033-01. 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

LabelerBeijing JUNGE Technology Co., Ltd.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code85212
First marketedJan 2025
Product typeHuman Otc Drug
Portfolio34 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?

Arthcal Turmeric Night Wrapping Mask is an over-the-counter monograph gel applied to the skin. It contains turmeric (Curcuma longa) and hydrolyzed bovine collagen, ingredients commonly used in skincare products intended to support skin appearance and texture. Turmeric is traditionally used for its antioxidant properties, while collagen functions as a moisturizing and skin-conditioning agent. This product is meant to be applied as a leave-on or rinse-off overnight mask.

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.

🧪 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.

  • 2 mL / 100 mL 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.
  • 0.1 mL / 100 mL UNII K72T3FS567
    Adenosine is a naturally occurring nucleoside compound. In medicines, it functions as an active pharmaceutical ingredient in some formulations, though when listed as an excipient it may serve as a buffering or stabilizing agent to maintain product stability and pH.
  • 65.9 mL / 100 mL 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.
  • 1 mL / 100 mL UNII PQ6CK8PD0R
    Ascorbic acid, also known as vitamin C, is a white crystalline powder. It serves as an antioxidant to prevent degradation of other ingredients and may also function as a preservative in the formulation.
  • 0.1 mL / 100 mL UNII K679OBS311
    Carboxymethylcellulose sodium is a plant-derived thickening agent made from cellulose. In medicines, it acts as a binder to hold ingredients together, a disintegrant to help the tablet break apart, or a thickener in liquids.
  • 5 mL / 100 mL UNII E107L85C40
    Dipropylene glycol is a clear liquid made from propylene glycol. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • 0.1 mL / 100 mL UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • 0.5 mL / 100 mL UNII M6FP5RZL0C
    Glycereth-6 laurate is a synthetic emulsifier made from glycerin and lauric acid. It helps mix oil and water-based ingredients together and may improve how the medicine spreads or absorbs.
  • 2 mL / 100 mL UNII ZR28QKN0WT
    Hydrolyzed elastin is a protein derived from animal connective tissue that has been broken down into smaller components. It acts as a humectant and skin-conditioning agent in formulations, helping to retain moisture and improve texture.
  • 0.1 mL / 100 mL UNII T4V6TWG28D
    A plant-derived thickening agent made from cellulose. It increases viscosity and helps form a gel or paste consistency in medications, and may serve as a binder or coating material in various formulations.
  • 2 mL / 100 mL UNII 6K23F1TT52
    Kojic acid is a naturally derived compound used as a preservative and antioxidant in medicines. It helps prevent spoilage and maintain product stability during storage.
  • 2 mL / 100 mL UNII 9E3P882579
    A seaweed-derived thickening and gelling agent made from brown kelp. It helps stabilize the medicine's texture and may be used as a binder or suspending agent to keep ingredients evenly mixed.
  • 1 mL / 100 mL UNII 76LN7P7UCU
    Lauryl glucoside is a mild plant-based cleansing agent made from coconut oil and glucose. It's used in medicines as a surfactant to help dissolve and distribute ingredients evenly throughout the formulation.
  • 0.1 mL / 100 mL UNII 806K32R50Z
    A synthetic liquid alcohol used in pharmaceuticals as a humectant and solvent. It helps keep the product moist and can dissolve or mix other ingredients together in liquid formulations.
  • 0.5 mL / 100 mL UNII 89NA02M4RX
    Pectin is a natural fiber extracted from fruit and plants. It's used in medicines as a thickener, binder, and gelling agent to create the right texture and help the product hold together.
  • 5 mL / 100 mL UNII 532B59J990
    Polyvinyl alcohol is a synthetic polymer made from plant-derived materials. It's used as a binder to hold ingredients together, a film-former in coatings, and a thickener in liquid formulations.
  • 1 mL / 100 mL UNII 6Y8XYV2NOF
    A waxy substance made by honeybees from plant resins and pollen. In medicines, it acts as a binder and coating agent to hold ingredients together and protect the product.
  • 1 mL / 100 mL UNII G2SH0XKK91
    Retinol is a form of vitamin A derived from animal sources or synthesized in a lab. In medicines, it may serve as an active therapeutic ingredient in some formulations, though when listed as an excipient it functions as a skin-conditioning agent or antioxidant to help stabilize the product.
  • 0.1 mL / 100 mL UNII 532IUT7IRV
    A salt derived from phosphoric acid, sodium metaphosphate acts as a buffer and sequestrant in medicines. It helps stabilize the product and prevent unwanted chemical reactions during storage.
  • 0.5 mL / 100 mL UNII C151H8M554
    A natural sugar derived from sugar cane or sugar beets. It's used as a sweetener, filler, and binder to improve taste, add bulk, and help hold tablet or capsule ingredients together.

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

The official label also statesAQUA DIPROPYLENE GLYCOL POLYVINYL ALCOHOL KOJIC ACID 1,2-HEXANEDIOL HYDROLYZED ELASTIN HYDROLYZED ALGIN RETINOL ASCORBIC ACID PROPOLIS EXTRACT LAURYL GLUCOSIDE GLYCERETH-6 LAURATE PECTIN SUCROSE CELLULOSE GUM HYDROXYETHYLCELLULOSE SODIUM METAPHOSPHATE OCTANEDIOL ETHYLHEXYLGLYCERIN ADENOSINE

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 gPer 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.
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
Arthcal TURMERIC NIGHT WRAPPING MASK 5 g/100mL; 5 g/100mL; 2000-5000 MW)this 85212-0033-01 Beijing 75 ml — — 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

🏛️
2025
On the market since
Jan 2025
📍
2026
Currently FDA-listed
1 year listed
🔒
·
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
85212-0033-01 You're viewing this 75 mL in 1 CONTAINER (85212-0033-1) 2025-01-01 Active

🧭 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 — Not published for this NDC No photo available yet for this listing.
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 85212-0033-1, 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: 85212-0033-01, written without dashes as 85212003301. 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 85212-0033-01, the first segment (85212) is the labeler code FDA assigned to Beijing JUNGE Technology Co., Ltd.; the middle segment (0033) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) 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 Beijing JUNGE Technology Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Beijing JUNGE Technology 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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 107 words ▾

Directions for Use Pre-Cleansing Routine After cleansing, apply toner to balance skin pH, followed by a moisturizer. Application Use a silicone brush or applicator to spread a thin, even layer over face, avoiding eye contours, lips, brows, and hairline. Translucent coverage is ideal.

Drying & Wear Time Allow mask to dry completely for 15 minutes before sleeping. Avoid touching the face to prevent transfer. Morning Removal Gently peel off the mask from the edges in the morning.

Rinse with lukewarm water if residue remains. Use a damp cotton pad on stubborn areas. Post-Treatment Follow with a calming serum or cream to lock in hydration and enhance radiance.

⏱️ Dosage and Administration 31 words ▾

STEP1 Cleanse and moisturize. STEP2 Apply the mask evenly to the face, avoiding eyes and mouth. STEP3 Let dry for 15 mins, then sleep. STEP4 Remove mask or rinse next morning.

⚠️ Warnings 138 words ▾

Patch Test Conduct a patch test 24 hours prior by applying a small amount behind ear or inner wrist. Discontinue if redness/itching occurs. Contraindications Avoid contact with eyes, open wounds, or active acne.

Rinse immediately if product enters eyes. × Compromised skin barrier (open wounds/post-op recovery) × Pathological skin conditions (rosacea/acute eczema/herpes flare-up) × Recent aesthetic procedures (＜6 weeks post-chemical peel/＜3 months post-laser) Storage & Shelf Life Store in a cool, dry place (below 25℃). Use within 6 months after opening. Special Populations Consult a physician before use if pregnant, breastfeeding, or with hypersensitive skin.

Keep away from children. Adverse Reactions Discontinue and apply a cool compress if irritation persists. Seek medical attention for severe reactions.

Drying & Overnight Care Allow the mask to dry completely before sleeping, and avoid contact with bedding or fabrics to prevent staining.

📦 Storage and Handling 7 words ▾

Keep in a dry and cool place.

🧪 Active Ingredient 5 words ▾

CURCUMA LONGA EXTRACT, HYDROLYZED COLLAGEN

🧪 Inactive Ingredients 31 words ▾

AQUA DIPROPYLENE GLYCOL POLYVINYL ALCOHOL KOJIC ACID 1,2-HEXANEDIOL HYDROLYZED ELASTIN HYDROLYZED ALGIN RETINOL ASCORBIC ACID PROPOLIS EXTRACT LAURYL GLUCOSIDE GLYCERETH-6 LAURATE PECTIN SUCROSE CELLULOSE GUM HYDROXYETHYLCELLULOSE SODIUM METAPHOSPHATE OCTANEDIOL ETHYLHEXYLGLYCERIN ADENOSINE

🎯 Purpose 5 words ▾

Wake Up to Dewy Skin

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 85212-0031-01 · Beijing 85212-0034-01 · Beijing →
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.