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Covex Antibacterial Bar Fresh Protection BENZALKONIUM CHLORIDE 1.3 mg/g Soap, 345 g — NDC 51209-0020-34 package photo

Covex Antibacterial Bar Fresh Protection BENZALKONIUM CHLORIDE 1.3 mg/g Soap, 345 g

by DALAN KIMYA ENDUSTRI ANONIM SIRKETI · 345 g in 1 PACKAGE (51209-020-34)
NDC 51209-0020-34
🏷️ FDA NDC (as labeled) 51209-020-34 billing pads the product segment with a zero
This package
Contains345 g Pack sizes3 compare ↓
Also comes in: 90 g 51209-0020-90 270 g 51209-0020-27
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 Benzalkonium Chloride (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Apr 8, 2026 — CGMP Deviations: product manufactured in the same facility under the same conditions as the product found to be contaminated (Blaine Labs Inc) · FDA recall D-0693-2026
Class II · Apr 8, 2026 — CGMP Deviations; product manufactured in the same facility under the same conditions as the product found to be contaminated (Blaine Labs Inc) · FDA recall D-0699-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0375-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0369-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0365-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0360-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 51209-020-34
Product NDC 51209-020
11-digit billing NDC 51209002034
RxCUI 2057666
UNII F5UM2KM3W7
UPC 0739835010082
Application # 505G(a)(3)
SPL Set ID bc18ed1f-1428-49c9-e053-2a95a90ac4c8
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-02-24
Route TOPICAL
Dosage form SOAP
Substance BENZALKONIUM CHLORIDE
Why two NDCs? The FDA registers this code as 51209-020-34 — 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 → 51209-0020-34. 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.

🏷️ RxNorm drug class

This medicine belongs to the Quaternary ammonium compounds class.

Drug family (ATC) Quaternary ammonium compounds, Medicated dressings with antiinfectives, Antiseptics
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

🏭 Manufacturer & labeler

LabelerDALAN KIMYA ENDUSTRI ANONIM SIRKETI
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code51209
First marketedFeb 2021
Product typeHuman Otc Drug
Portfolio13 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?

Covex Antibacterial Bar is an over-the-counter bar soap containing benzalkonium chloride, an antimicrobial agent typically used in cleansing products to help reduce bacteria on the skin. This product is marketed under FDA's established rules for antibacterial soaps and is applied topically during routine washing. Benzalkonium chloride functions as a broad-spectrum antiseptic commonly found in hand soaps and personal hygiene products.

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 7X6O37OK2I
    A synthetic fragrance compound used as a flavoring agent or aromatic component in medicines. It adds pleasant taste or smell to make the medication more acceptable to patients.
  • UNII WAO5MNK9TU
    Benzyl salicylate is a fragrant chemical compound used as a flavor and scent ingredient in medicines. It helps mask unpleasant tastes or odors in liquid or oral formulations.
  • UNII GC844VRD7E
    A synthetic fatty acid ester derived from plant oils and lactic acid. It acts as an emulsifier and solvent to help mix oil and water-based ingredients and improve how the medicine dissolves or spreads in the body.
  • UNII 81G7704MYR
    A synthetic brightening agent derived from biphenyl compounds. It's used as an optical whitener and colorant in tablets and capsules to make medicines appear brighter and more visually appealing.
  • UNII MP1J8420LU
    A salt derived from edetic acid that binds to trace metals in medicines. It serves as a chelating agent and preservative to prevent metal-catalyzed breakdown of the drug and extend shelf life.
  • UNII M2F465ROXU
    A phosphorus-containing compound used as a chelating agent and water softener in pharmaceutical formulations. It helps prevent mineral buildup and stabilizes the medicine by binding to metal ions that could otherwise degrade the product.
  • 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 9XP4LC555B
    A fragrance compound derived from natural plant sources or made synthetically. It's added to medicines as a flavoring agent to mask bitter tastes and improve how the medicine smells and tastes.
  • UNII GFD7C86Q1W
    A natural oil extracted from citrus peels, (+)-limonene is used as a flavoring agent and solvent in medicines. It helps dissolve active ingredients and provides a lemon or orange taste.
  • UNII D81QY6I88E
    Linalool is a natural fragrant oil found in plants like lavender and citrus. It's used in medicines as a flavoring agent and to mask unpleasant tastes or smells.
  • 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 6H91L1NXTW
    A processed palm kernel oil derivative used as an emulsifier and surfactant in medications. It helps mix oil and water-based ingredients together and improves how the medicine spreads and dissolves in the body.
  • UNII S0A6004K3Z
    Sodium palmate is a salt made from palm oil. It acts as an emulsifier and surfactant in medicines, helping mix ingredients that normally don't blend well together and improving product texture and consistency.
  • UNII 07RIK6QMEW
    A fatty substance derived from beef tallow used as an emulsifier and cleansing agent. It helps blend oil and water-based ingredients in the formulation and may improve the product's texture and consistency.
  • UNII 15FIX9V2JP
    Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.
  • 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 SOI2LOH54Z
    Zinc oxide is a white mineral powder used in medicines as a protective barrier agent and color additive. It helps shield skin in topical products and may also serve as a filler or opacifying ingredient.

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

The official label also statesSodium Tallowate, Sodium Palmate, Water, Sodium Palm Kernelate, Fragrance, Sodium Chloride, Glycerine, Zinc Oxide, C12-15 Alkyl Lactate, Titanium Dioxide, Tetrasodium EDTA, Etidronic Acid, Disodium Distyrylbiphenyl Disulfonate, Alpha-Isomethyl Ionone, Hexyl Cinnamal, Linalool, Limonene, Benzyl Salicylate.

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: 90 g 270 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
Covex Antibacterial Bar Active Protection 1.3 mg/g 51209-0017-00 DALAN 115 g — — FDA listed —
Covex Antibacterial Bar Cool Protection 1.3 mg/g 51209-0018-00 DALAN 115 g — — FDA listed —
Covex Antibacterial Bar Fresh Protection 1.3 mg/gthis 51209-0020-34 DALAN 345 g — — FDA listed —
Covex Antibacterial Bar Active Protection 1.3 mg/g 51209-0021-27 DALAN 270 g — — FDA listed —
Covex Antibacterial Bar Cool Protection 1.3 mg/g 51209-0022-27 DALAN 270 g — — FDA listed —
American Red Cross Antibacterial Bar 1.3 mg/g 51628-0034-00 My 85 g — — FDA listed —
Dove .13 g/100g 64942-1846-01 Conopco 212 g — — FDA listed —
Dove .13 g/100g 64942-2455-01 Conopco 106 g — — FDA listed —
Dove .13 g/100g 64942-2468-01 Conopco 850 g — — FDA listed —
Terramed Just Think Comfort Armor Antibacterial Cleansing Bar .13 g/100g 83004-0033-01 Rida 120 g — — FDA listed —
Obstetrical Towelette 1.3 mg/g 34645-0015-01 Jianerkang 1 patch — — FDA listed —
BZK Antiseptic Towelette Non-Sterile 1.3 mg/g 34645-0017-01 Jianerkang 1 patch — — FDA listed —
BZK Antiseptic Towelette Sterile 1.3 mg/g 34645-0018-01 Jianerkang 1 patch — — FDA listed —
Cleansing Towelette 1.3 mg/g 34645-0019-01 Jianerkang 1 patch — — FDA listed —
BZK Antiseptic Wipe 1.3 mg/g 59050-0264-01 Changzhou 1 patch — — FDA listed —
Antiseptic BZK Towelette 1.3 mg/g 63517-0501-83 Cardinal 100 pouches — — FDA listed —
Antiseptic Towelette TOALLITAS ANTISEPTICAS 1.3 mg/g 84219-0004-00 M-star 1 patch — — FDA listed —
MyMedic Antiseptic Towelette 1.3 mg/g 59050-0273-01 Changzhou 1 patch — — FDA listed —
BZK Antiseptic Wipe 1.3 mg/g 59050-0262-01 Changzhou 1 patch — — FDA listed —
Club Wipes Sanitizing Wipes Lemon Scent 1.3 mg/g 78940-0010-12 Golden 1200 patches — — Discontinued —
CLUB Wipes Sanitizing Wipes for Hands 1.3 mg/g 42326-0099-00 Petra 1500 patches — — FDA listed —
Health E Wipes, Lemon Scent 1.3 mg/g 78940-0011-10 Golden 1000 patches — — Discontinued —
Antiseptic Towelette 1.3 mg/g 82264-0008-00 UNCHARTED 10 applicators — — FDA listed —
Genuine First Aid Antiseptic Towelette 1.3 mg/g 50814-0081-00 GFA 25 g — — FDA listed —
Antiseptic Towelette 1.3 mg/g 82996-0004-01 Hubei 1 pouch — — FDA listed —
My-Shield Sanitizing Hand Wipes 1.3 mg/g 71884-0010-20 ENVIRO 960 patches — — FDA listed —
Urgent First Aid BZK Antiseptic Wipe 1.3 mg/g 59050-0275-01 Changzhou 1 patch — — 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

🏛️
2021
On the market since
Feb 2021
📍
2026
Currently FDA-listed
5 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 Covex Antibacterial Bar Fresh Protection (this brand).

Top reported reactions

Drug Hypersensitivity118
Condition Aggravated114
Arthralgia112
Musculoskeletal Stiffness111
Pain In Extremity111
Infection110
Hepatotoxicity108

Age at onset

Infant1
Adolescent3
Adult36
Elderly10

Reporter sex

331 reports
Male · 28%
Female · 72%
Unknown · 0%

Serious outcomes

Death25
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 77 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
51209-0020-27 270 g in 1 PACKAGE (51209-020-27) 2021-02-24 Active
51209-0020-34 You're viewing this 345 g in 1 PACKAGE (51209-020-34) 2021-02-24 Active
51209-0020-90 90 g in 1 BOX (51209-020-90) 2021-02-24 Active

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

Pack size FAQ

What quantity is in NDC 51209-0020-34?
NDC 51209-0020-34 contains 345 g — 345 g in 1 package.
What is the difference between NDC 51209-0020-34 and NDC 51209-0020-90?
Both are Covex Antibacterial Bar Fresh Protection BENZALKONIUM CHLORIDE 1.3 mg/g Soap — the drug itself is identical. NDC 51209-0020-34 is the 345 g package, while NDC 51209-0020-90 is the 90 g package.
What NDC number is used to bill for this package of Covex Antibacterial Bar Fresh Protection BENZALKONIUM CHLORIDE 1.3 mg/g Soap?
Bill NDC 51209-0020-34 — the 11-digit billing format is 51209002034. 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 51209-020-34, 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: 51209-0020-34, written without dashes as 51209002034. 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 51209-0020-34, the first segment (51209) is the labeler code FDA assigned to DALAN KIMYA ENDUSTRI ANONIM SIRKETI; the middle segment (0020) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (34) 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 DALAN KIMYA ENDUSTRI ANONIM SIRKETI. 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 90 g (51209-0020-90), 270 g (51209-0020-27). 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?
DALAN KIMYA ENDUSTRI ANONIM SIRKETI 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 9 words ▾

Uses for handwashing to decrease bacteria on the skin

⏱️ Dosage and Administration 18 words ▾

Directions Wet hands and forearms. Apply to hands and forearms. Scrub thoroughly for 60 seconds. Rinse and repeat

⚠️ Warnings 56 words ▾

Warnings For external use only When using this product Do not use in the eyes. Stop use and ask a doctor if irritation and redness develop. If condition persists for more than 72 hours consult a doctor. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 7 words ▾

Active ingredients Benzalkonium Chloride 0.13% Purpose Antibacterial

🧪 Inactive Ingredients 36 words ▾

Inactive ingredients: Sodium Tallowate, Sodium Palmate, Water, Sodium Palm Kernelate, Fragrance, Sodium Chloride, Glycerine, Zinc Oxide, C12-15 Alkyl Lactate, Titanium Dioxide, Tetrasodium EDTA, Etidronic Acid, Disodium Distyrylbiphenyl Disulfonate, Alpha-Isomethyl Ionone, Hexyl Cinnamal, Linalool, Limonene, Benzyl Salicylate.

🎯 Purpose 2 words ▾

Purpose Antibacterial

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 51209-0018-00 · DALAN 51209-0021-27 · DALAN →
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.