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FIND BICHON CLEANSING MASK GLYCERIN 1 g/100g Liquid, 20 g — NDC 70441-0005-01 package photo

FIND BICHON CLEANSING MASK GLYCERIN 1 g/100g Liquid, 20 g

by Pioom Cosmetic Co.,ltd · 20 g in 1 POUCH (70441-0005-1)
NDC 70441-0005-01
🏷️ FDA NDC (as labeled) 70441-0005-1 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

⚠️
Other active recalls for Glycerin (different manufacturers) — 4 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Apr 27, 2026 — Lack of Assurance of Sterility: The recall is being initiated out of an abundance of caution following FDA observations noted during a recent inspection of Excelvision. (Oasis Medical, Inc.) · FDA recall D-0525-2026
Class II · Apr 20, 2026 — Lack of Assurance of Sterility (SCOPE HEALTH) · FDA recall D-0499-2026
Class II · Mar 25, 2026 — Lack of Assurance of Sterility (Preferred Pharmaceuticals, Inc.) · FDA recall D-0443-2026
Class II · Mar 3, 2026 — Lack of Assurance of Sterility (K.C. Pharmaceuticals, Inc) · FDA recall D-0411-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 70441-0005-1
Product NDC 70441-0005
11-digit billing NDC 70441000501
UNII PDC6A3C0OX
SPL Set ID 50b7db48-7b55-6df4-e054-00144ff88e88
Established class (EPC) Non-Standardized Chemical Allergen
Physiologic effect Increased Histamine Release; Cell-mediated Immunity; Increased IgG Production
Chemical class Allergens; Glycerol
DEA schedule Non-controlled
Marketing category UNAPPROVED DRUG OTHER
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2017-05-01
Route TOPICAL
Dosage form LIQUID
Substance GLYCERIN
Why two NDCs? The FDA registers this code as 70441-0005-1 — 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 → 70441-0005-01. 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

LabelerPioom Cosmetic Co.,ltd
Labeler code70441
First marketedMay 2017
Product typeHuman Otc Drug
Portfolio4 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 a topical liquid cleansing mask containing glycerin as its active ingredient. Glycerin is commonly used in skincare products as a humectant, meaning it helps draw moisture into the skin and is often included in cleansers and masks intended to hydrate and soften the skin. This product is marketed as an unapproved drug and has not received FDA approval through a standard drug application process.

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.

  • 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 inactive ingredient listed in the exact product block matched to this NDC.

The official label also statesWater Cocamidopropyl Betaine Sodium Lauryl Sulfate Methyl Perfluorobutyl Ether Methyl Perfluoroisobutyl Ether Cocamide DEA Propylene glycol Disodium Cocoamphodiacetate Acrylates Copolymer Colloidal Gold Citrus Paradisi (Grapefruit) Fruit Extract Melaleuca Alternifolia (Tea Tree) Extract Salvia Officinalis (Sage) Leaf Extract Lavandula Angustifolia (Lavender) Flower Extract Rosmarinus Officinalis (Rosemary) Extract Chamomilla Recutita (Matricaria) Flower Extract Cymbopogon Schoenanthus Extract Panthenol Cholesterol Beta-Sitosterol 1,2-Hexanediol Choleth-24 Ceteth-24 Biotin Ascorbyl Tetraisopalmitate Niacinamide Potassium Cetyl Phosphate Tocopheryl Acetate Glyceryl Linoleate Glyceryl Linolenate Glyceryl Arachidonate Dimethicone Cyclomethicone Ubiquinone Sodium Chloride Citric Acid Phenoxyethanol Disodium EDTA Propanediol Caprylhydroxamic Acid Fragrance

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 mLPer 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
Find Bichon Cleansing Mask 1 g/100gthis 70441-0005-01 Pioom 20 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

🏛️
2017
On the market since
May 2017
📍
2026
Currently FDA-listed
9 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.

🔬 Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for FIND BICHON CLEANSING MASK (this brand).

Top reported reactions

Macular Degeneration598
Constipation440
Pain400
Nausea322
Pyrexia308
Malaise275
Weight Decreased268

Age at onset

Neonate3
Infant8
Child11
Adolescent7
Adult144
Elderly323

Reporter sex

2,562 reports
Reports over time (by year) — tap or hover for the count & year
2020 2022 2024 2026 470 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
70441-0005-01 You're viewing this 20 g in 1 POUCH (70441-0005-1) 2017-05-01 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Marketed without an FDA application

Listed without an FDA application

This product's marketing category indicates it is marketed without an approved FDA application (no NDA, ANDA, or BLA on file). Having an NDC does not by itself establish FDA approval — the NDC Directory is a listing system, not an approval decision. Approval-linked data such as Orange Book therapeutic-equivalence ratings therefore does not apply.

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 "Unapproved Drug Other". 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 70441-0005-1, 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: 70441-0005-01, written without dashes as 70441000501. 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 70441-0005-01, the first segment (70441) is the labeler code FDA assigned to Pioom Cosmetic Co.,ltd; the middle segment (0005) 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 Pioom Cosmetic Co.,ltd. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Pioom Cosmetic 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 55 words ▾

Clean the skin thoroughly before using this product. Apply the mask over cleansed face and leave on for 5 to 10 minutes, allowing the sparkling bubbles to fully rise. Peel off the mask, and gently massage the skin using the residual bubbles. Finish by rinsing with warm water. For best results, repeat twice a week.

⏱️ Dosage and Administration 4 words ▾

for external use only

⚠️ Warnings 105 words ▾

1. If the following symptoms occur after product use, stop using the product immediately and consult a dermatologist (continuous use can exacerbate the symptoms). 1) Occurrence of red spots, swelling, itchiness, and other skin irritation 2) If the symptoms above occur after the application area is exposed to direct sunlight 2.

Do not use on open wounds, eczema, and other skin irritations 3. Precaution for Storage and Handling 1) Close the lid after use 2) Keep out of reach of infants and children 3) Do not to store in a place with high/low temperature and exposed to direct sunlight 4. Use as avoiding eye areas.

🧪 Active Ingredient 1 words ▾

GLYCERIN

🧪 Inactive Ingredients 89 words ▾

Water Cocamidopropyl Betaine Sodium Lauryl Sulfate Methyl Perfluorobutyl Ether Methyl Perfluoroisobutyl Ether Cocamide DEA Propylene glycol Disodium Cocoamphodiacetate Acrylates Copolymer Colloidal Gold Citrus Paradisi (Grapefruit) Fruit Extract Melaleuca Alternifolia (Tea Tree) Extract Salvia Officinalis (Sage) Leaf Extract Lavandula Angustifolia (Lavender) Flower Extract Rosmarinus Officinalis (Rosemary) Extract Chamomilla Recutita (Matricaria) Flower Extract Cymbopogon Schoenanthus Extract Panthenol Cholesterol Beta-Sitosterol 1,2-Hexanediol Choleth-24 Ceteth-24 Biotin Ascorbyl Tetraisopalmitate Niacinamide Potassium Cetyl Phosphate Tocopheryl Acetate Glyceryl Linoleate Glyceryl Linolenate Glyceryl Arachidonate Dimethicone Cyclomethicone Ubiquinone Sodium Chloride Citric Acid Phenoxyethanol Disodium EDTA Propanediol Caprylhydroxamic Acid Fragrance

🎯 Purpose 5 words ▾

Dead skin cell, pore control

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 70441-0004-01 · Pioom 70444-7001-09 · Helixor →
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.