Home › NDC Lookup › Ingredients › Turmeric Kojic Acid › 85212-0003-01
🫧image loading
(from DailyMed)

FluMisch Turmeric Kojic Acid Facial Cleanser 5 g/100mL Aerosol, Foam, 120 mL

by Beijing JUNGE Technology Co., Ltd. · 120 mL in 1 BOTTLE (85212-0003-1)
NDC 85212-0003-01
🏷️ FDA NDC (as labeled) 85212-0003-1 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) 85212-0003-1
Product NDC 85212-0003
11-digit billing NDC 85212000301
UNII 856YO1Z64F
Application # 505G(a)(3)
SPL Set ID 2dee6804-1afd-a539-e063-6294a90a7567
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-09-01
Route EXTRACORPOREAL
Dosage form AEROSOL, FOAM
Substance CURCUMA LONGA (TURMERIC) ROOT POWDER
Why two NDCs? The FDA registers this code as 85212-0003-1 — 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 → 85212-0003-01. 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 marketedSep 2024
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?

FluMisch Turmeric Kojic Acid Facial Cleanser is an over-the-counter foaming aerosol product intended for topical use on the skin. The active ingredient is turmeric root powder, which is commonly used in skincare products for its potential antioxidant and anti-inflammatory properties. This product is marketed under the FDA's over-the-counter monograph rules for skin-cleansing preparations rather than as an individually approved drug application. The foam formulation is designed to be applied directly to facial skin as part of a cleansing routine.

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.

  • 1 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.
  • 66.45 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.
  • 5 mL / 100 mL 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.
  • 0.2 mL / 100 mL 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.
  • 0.1 mL / 100 mL UNII 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • 2 mL / 100 mL UNII Z17H97EA6Y
    A plant-derived mild cleanser made from natural sugars and oils. It acts as an emulsifier and surfactant to help mix water and oil-based ingredients together in the medicine.
  • 3 mL / 100 mL UNII MBK0CP8F5A
    Disodium cocoyl glutamate is a mild cleanser derived from coconut oil and amino acids. It acts as a surfactant and emulsifier in medicines, helping to mix oil and water-based ingredients together and improve how the product spreads or absorbs.
  • 5 mL / 100 mL 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.
  • 0.5 mL / 100 mL 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.
  • 1 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.
  • 0.15 mL / 100 mL UNII QC5HRP6AG0
    A plant-derived ingredient from Ophiopogon japonicus seeds, traditionally used in herbal formulations. In medicines, it may serve as a natural filler or binder to help hold tablet or capsule contents together.
  • 0.15 mL / 100 mL UNII 5ZC110ZY2H
    A juice extracted from the prickly pear fruit, used as a natural sweetener, flavoring agent, and colorant in medications. It adds taste and appearance appeal while contributing minimal active effects.
  • 0.2 mL / 100 mL UNII 90TF85HH91
    A fatty substance made from glycerin and stearic acid. It works as an emulsifier to help mix oil and water-based ingredients together in the medicine, and may also help with texture and consistency.
  • 0.2 mL / 100 mL UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • 0.5 mL / 100 mL UNII 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
  • 2 mL / 100 mL UNII NCX1UU2D33
    Sodium lauroyl glutamate is a mild cleanser derived from coconut oil and the amino acid glutamate. In medicines, it acts as a surfactant and emulsifier to help mix oily and watery ingredients and improve how the product spreads or dissolves.
  • 5 mL / 100 mL UNII 632GS99618
    Sodium lauroyl sarcosinate is a mild, plant-derived cleaning agent used in medicines as a surfactant and emulsifier. It helps mix oil and water-based ingredients and may aid tablet disintegration.
  • 1 mL / 100 mL UNII 469OTG57A2
    Sodium pyrrolidone carboxylate is a synthetic polymer derived from pyrrolidone chemistry. It functions as a solubilizer and binder in medications, helping dissolve poorly water-soluble drugs and hold tablet ingredients together.
  • 1 mL / 100 mL UNII LN8DW52UVL
    Sodium polyglutamate is a synthetic polymer made from the sodium salt of glutamic acid. It acts as a binder and thickening agent to help hold tablet ingredients together and improve the texture of liquid formulations.
  • 0.15 mL / 100 mL UNII IYR6K8KQ5K
    A plant extract from sophora flavescens root used as a natural colorant and flavoring agent in medicines. It may also help preserve the product and provide texture.
  • 0.2 mL / 100 mL UNII 274KW0O50M
    Sucrose stearate is a compound made from sugar and stearic acid (a fatty substance). It works as an emulsifier and surfactant to help mix oils and water-based ingredients together in the medicine.
  • 0.2 mL / 100 mL UNII B8WCK70T7I
    Trehalose is a natural sugar made from two glucose molecules linked together. It's used in medicines as a filler to add bulk, a sweetener for taste, and a stabilizer to help keep active ingredients effective during storage.

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

The official label also statesAQUA-GLYCERIN-BUTYLENE GLYCOL-SODIUM LAUROYL SARCOSINATE-DISODIUM COCOYL GLUTAMATE-DECYL GLUCOSIDE-SODIUM LAUROYL GLUTAMATE-KOJIC ACID-SODIUM PCA-1,2-HEXANEDIOL-CHRYSANTHELLUM INDICUM EXTRACT-SODIUM POLYGLUTAMATE-OLEA EUROPAEA (OLIVE) FRUIT OIL-SODIUM CHLORIDE-HYDROXYACETOPHENONE-PROPYLENE GLYCOL-CERAMIDE 3-POLYGLYCERYL-10 STEARATE-TREHALOSE-BAKUMONDOU EKISU-OPUNTIA FICUS-INDICA FRUIT EXTRACT-SOPHORA FLAVESCENS ROOT EXTRACT-CITRIC ACID-HYDROGENATED LECITHIN-SUCROSE STEARATE

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
FluMisch Turmeric Kojic Acid Facial Cleanser 5 g/100mLthis 85212-0003-01 Beijing 120 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

🏛️
2024
On the market since
Sep 2024
📍
2026
Currently FDA-listed
2 years 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
85212-0003-01 You're viewing this 120 mL in 1 BOTTLE (85212-0003-1) 2024-09-01 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 85212-0003-1, 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: 85212-0003-01, written without dashes as 85212000301. 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 85212-0003-01, the first segment (85212) is the labeler code FDA assigned to Beijing JUNGE Technology Co., Ltd.; the middle segment (0003) 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 4 words ▾

For cleansing facial skin

⏱️ Dosage and Administration 73 words ▾

Pump an adequate amount of the mousse into your hands. The rich foam will form instantly Gently massage the foam onto damp skin in circular motions, focusing on areas prone to dirt and oil, like the forehead, nose, and chin Rinse thoroughly with lukewarm water and pat dry with a clean towel For best results, use twice daily—morning and evening. Follow with your favorite toner, serum, and moisturizer for a complete skincare routine.

⚠️ Warnings 12 words ▾

For external use only. Please keep out of children. Do not swallow.

📦 Storage and Handling 35 words ▾

Before use, read all information on carton and enclosed leaflet Store at controlled room temperature 20° to 25℃ (68° to 77°F).Do not incinerate container, Do not expose to heat or store attemperature abowe 120°F (49°C).

🧪 Active Ingredient 4 words ▾

TURMERIC & KOJIC ACID

🧪 Inactive Ingredients 32 words ▾

AQUA-GLYCERIN-BUTYLENE GLYCOL-SODIUM LAUROYL SARCOSINATE-DISODIUM COCOYL GLUTAMATE-DECYL GLUCOSIDE-SODIUM LAUROYL GLUTAMATE-KOJIC ACID-SODIUM PCA-1,2-HEXANEDIOL-CHRYSANTHELLUM INDICUM EXTRACT-SODIUM POLYGLUTAMATE-OLEA EUROPAEA (OLIVE) FRUIT OIL-SODIUM CHLORIDE-HYDROXYACETOPHENONE-PROPYLENE GLYCOL-CERAMIDE 3-POLYGLYCERYL-10 STEARATE-TREHALOSE-BAKUMONDOU EKISU-OPUNTIA FICUS-INDICA FRUIT EXTRACT-SOPHORA FLAVESCENS ROOT EXTRACT-CITRIC ACID-HYDROGENATED LECITHIN-SUCROSE STEARATE

🎯 Purpose 2 words ▾

facial cleansing

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 85212-0002-01 · Beijing 85212-0004-01 · 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.