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CharmTex All in One Antibacterial Shave Gel Body Wash BENZETHONIUM CHLORIDE .1 g/100g Shampoo, 9.6 g — NDC 85420-0003-06 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

CharmTex All in One Antibacterial Shave Gel Body Wash BENZETHONIUM CHLORIDE .1 g/100g Shampoo, 9.6 g — NDC 85420-003-06 (Billing 85420-0003-06)

by Liufangjing Biotechnology (Yangzhou) Co., Ltd · 9.6 g in 1 PACKET

This is a package of 9.6 g of CharmTex All in One Antibacterial Shave Gel Body Wash BENZETHONIUM CHLORIDE .1 g/100g Shampoo from Liufangjing Biotechnology (Yangzhou) Co., Ltd, marketed since Jun 2025 and currently FDA-listed. It is this product's only package size.

NDC 85420-0003-06
🏷️ FDA NDC (as labeled) 85420-003-06 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed 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

NDC database record

One package, one record: these facts belong to NDC 85420-003-06 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
85420 labeler · 003 product · 06 package
Package marketed since
Jun 1, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 8542000306 1
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 85420-003-06
Product NDC 85420-003
11-digit billing NDC 85420000306
UNII PH41D05744
Application # M005
SPL Set ID a7433f39-a8d9-4c78-864d-d7ef193a7daf
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-06-01
Route TOPICAL
Dosage form SHAMPOO
Substance BENZETHONIUM CHLORIDE
Why two NDCs? The FDA registers this code as 85420-003-06 — 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 → 85420-0003-06. 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.

Clinical

🧪 What is this product?

This is a topical shampoo product marketed as an antibacterial body wash and shave gel. The active ingredient is benzethonium chloride, an antimicrobial agent that is commonly used in over-the-counter soaps and cleansing products to help reduce bacteria on the skin. This product is regulated as an OTC monograph drug, meaning it follows FDA's established rules for its category rather than undergoing individual product approval. It is applied to the skin during bathing or grooming.

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.

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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
85420-0003-06 You're viewing this Main listing 9.6 g in 1 PACKET 2025-06-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Meridian Antibacterial Deodorant .1 g/100g 71035-0004-01 Yangzhou 1000 pouches — — FDA listed —
Meridian Unwarpped Antibacterial Deodorant 3 Oz .1 g/100g 72797-0005-01 Yangzhou 85 g — — FDA listed —
Amerfresh Antibacterial Deodorant .1 g/100g 85420-0002-01 Liufangjing 1 applicator — — FDA listed —
BobBarker antibacterial wrapped body .1 g/100g 72797-0001-01 Yangzhou 11.06 g — — FDA listed —
Meridian Warpped Antibacterial Deodorant 3 Oz .1 g/100g 72797-0007-01 Yangzhou 85 g — — FDA listed —
Meridian Warpped Antibacterial Deodorant 1.25 .1 g/100g 72797-0008-01 Yangzhou 29 g — — FDA listed —
CharmTex All in One Antibacterial Shave Gel Body Wash .1 g/100gthis 85420-0003-06 Liufangjing 9.6 g — — FDA listed —
Meridian Warpped Antibacterial Deodorant 0.5 .1 g/100g 72797-0006-01 Yangzhou 11 g — — FDA listed —
Meridian Warpped Antibacterial Deodorant 3 .1 g/100g 72797-0009-01 Yangzhou 75 g — — FDA listed —
Meridian Unwarpped Antibacterial Deodorant 1.5 .1 g/100g 72797-0002-01 Yangzhou 32 g — — FDA listed —
CharmTex Lightly Scented Antibacterial .1 g/100g 85420-0004-01 Liufangjing 1 applicator — — FDA listed —
Meridian Unwrapped Antibacterial Deodorant .1 g/100g 85420-0005-01 Liufangjing 500 applicators — — FDA listed —
Meridian Unwrapped Antibacterial Deodorant .1 g/100g 71035-0003-01 Yangzhou 1000 applicators — — FDA listed —
Meridian Unwarpped Antibacterial Deodorant 0.5 .1 g/100g 72797-0003-01 Yangzhou 11 g — — FDA listed —
Meridian Unwarpped Antibacterial Deodorant 3 .1 g/100g 72797-0004-01 Yangzhou 75 g — — FDA listed —
CharmTex All in One Antibacterial Shave Gel Body Wash .1 g/100g 87866-0001-01 Yangzhou 10 g — — FDA listed —
Meridian Unwrapped Antibacterial Deodorant .1 g/100g 87866-0002-01 Yangzhou 500 applicators — — FDA listed —
Meridian Antibacterial Deodorant .1 g/100g 87866-0003-01 Yangzhou 500 pouches — — FDA listed —
CharmTex Lightly Scented Antibacterial .1 g/100g 87866-0004-01 Yangzhou 1 applicator — — 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
Jun 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.

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 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.
  • UNII 92005F972D
    A foaming and thickening agent derived from coconut oil. It's used in liquid medicines to improve texture, help distribute active ingredients evenly, and create a pleasant consistency for easier swallowing or application.
  • UNII 5OCF3O11KX
    A plant-derived surfactant made from coconut oil. It helps mix oil and water ingredients together in the formulation and can improve how the medicine spreads or feels on the skin.
  • UNII BYR0546TOW
    DMDM hydantoin is a preservative chemical used to prevent the growth of bacteria and fungi in medicines. It helps keep the product safe and stable throughout its shelf life.
  • 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.
  • UNII 368GB5141J
    A detergent and foaming agent derived from coconut or palm oil. In medications, it helps break down and mix oil and water-based ingredients, aids in tablet disintegration, and improves how the drug dissolves and spreads in the mouth or digestive system.
  • 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.

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

The official label also statesWater, Cocamidepropyl Betain, Sodium Lauyl Sufate, Cocamide Dea, Sodium Chloride, DMDM Hydantoin, Frgrance, Citric Acid

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.

Manufacturer & labeler

LabelerLiufangjing Biotechnology (Yangzhou) Co., Ltd
FDA applicationM005 (OTC MONOGRAPH DRUG)
Labeler code85420
First marketedJun 2025
Product typeHuman Otc Drug
Portfolio6 products on file

More NDCs from Liufangjing Biotechnology (Yangzhou) Co., Ltd labeler code 85420

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.

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 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 30 words ▾

Use As shave gel: Smooth skin when do shaving and help reduce bacteria As body wash: Body cleaning to help reduce bateria As shampoo: Hair cleaning to help redice baterial

⏱️ Dosage and Administration 47 words ▾

Directions As shave gel: Wet skin and squeeze gel onto finger tips. Spread gel evenly on skin and shave As body wash: Squeeze body wash onto hands or wash cloth. Apply, lather, and rinse As shampoo: Wet hair, apply shampoo, work up a rich lather and rinse.

⚠️ Warnings 20 words ▾

Warnings For external use only Keep out of eyes, ears, or mouth. In case of contect flush eyes with water

🧪 Active Ingredient 5 words ▾

Active Ingredient Benzethonium Chloride 0.1%

🧪 Inactive Ingredients 17 words ▾

Inactive ingredients Water, Cocamidepropyl Betain, Sodium Lauyl Sufate, Cocamide Dea, Sodium Chloride, DMDM Hydantoin, Frgrance, Citric Acid

🎯 Purpose 2 words ▾

Purpose Antiseptic

📄 Stop Use and Ask a Doctor If 20 words ▾

Stop use and ask a doctor if irritation and redness develop, or if condition persists for more than 72 hours

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Package Label / Principal Display Panel 2 words ▾

image description

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 CharmTex All in One Antibacterial Shave Gel Body Wash (this brand).

Top reported reactions

Nausea23
Hypersensitivity20
Headache18
Therapeutic Product Effect Decreased17
Contraindicated Product Administered10
Diarrhoea6
Death5

Age at onset

Child1
Adult7
Elderly13

Reporter sex

85 reports
Male · 38%
Female · 62%

Serious outcomes

Hospitalization44
Death17
Life-threatening3
Disabling3
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 12 2
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.

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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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 Liufangjing Biotechnology (Yangzhou) Co., Ltd. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Liufangjing Biotechnology (Yangzhou) 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.
← 85420-0002-01 · Liufangjing 85420-0004-01 · Liufangjing →
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.