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Dial Antibacterial Bar .1 g/100g Soap, 678 g — NDC 54340-0274-04 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Dial Antibacterial Bar .1 g/100g Soap, 678 g — NDC 54340-274-04 (Billing 54340-0274-04)

by Henkel Corporation · 678 g in 1 CELLO PACK

This is a package of 678 g of Dial Antibacterial Bar .1 g/100g Soap from Henkel Corporation, no longer marketed (first marketed Jul 2017), no longer in the FDA NDC Directory.

NDC 54340-0274-04
🏷️ FDA NDC (as labeled) 54340-274-04 billing pads the product segment with a zero
This package
Contains678 g Pack sizes13 compare ↓
Product page 54340-0274-01 Also comes in: 4 cellos 54340-274-11 8 cellos 54340-274-14 12 cellos 54340-274-13 180 g 54340-274-01 339 g 54340-274-02 339 g 54340-274-09 452 g 54340-274-03 540 g 54340-274-05 904 g 54340-274-10 940 g 54340-274-06 1130 g 54340-274-07 1356 g 54340-274-08
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 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 54340-274-04 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
54340 labeler · 274 product · 04 package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 5434027404 2
FDA record last changed
Jul 24, 2026
⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 54340-274-04
Product NDC 54340-274
11-digit billing NDC 54340027404
RxCUI 1926450
UNII F5UM2KM3W7
Application # 505G(a)(3)
SPL Set ID 568518c8-e327-45a7-e054-00144ff8d46c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm
Marketing start 2017-07-01
Route TOPICAL
Dosage form SOAP
Substance BENZALKONIUM CHLORIDE
Quick answers
  • RxCUI (RxNorm): 1926450
Why two NDCs? The FDA registers this code as 54340-274-04 — 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 → 54340-0274-04. 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.

Clinical

🧪 What is this product?

Dial Antibacterial Bar is a topical soap containing benzalkonium chloride, an antimicrobial agent. This product is marketed as an over-the-counter monograph drug, meaning it follows FDA's established guidelines for antibacterial bar soaps rather than undergoing individual product review. Benzalkonium chloride is typically used in soaps to help reduce bacteria on the skin during washing. This bar soap is intended for routine cleansing and hygiene purposes.

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 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: 4 cellos 8 cellos 12 cellos 180 g 339 g 339 g 452 g 540 g 904 g 940 g 1130 g 1356 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
54340-0274-01 54340-274-01 Main listing 180 g in 1 CELLO PACK 2017-07-01 — Discontinued by firm
54340-0274-02 54340-274-02 339 g in 1 CELLO PACK 2017-07-01 — Active
54340-0274-03 54340-274-03 452 g in 1 CELLO PACK 2017-07-01 — Active
54340-0274-04 You're viewing this 678 g in 1 CELLO PACK 2017-07-01 — Discontinued by firm
54340-0274-05 54340-274-05 540 g in 1 CELLO PACK 2017-07-01 — Discontinued by firm
54340-0274-06 54340-274-06 940 g in 1 CELLO PACK 2017-07-01 — Discontinued by firm
54340-0274-07 54340-274-07 1130 g in 1 CELLO PACK 2017-07-01 — Discontinued by firm
54340-0274-08 54340-274-08 1356 g in 1 CELLO PACK 2017-07-01 — Discontinued by firm
54340-0274-09 54340-274-09 339 g in 1 CELLO PACK 2023-01-31 — Discontinued by firm
54340-0274-10 54340-274-10 904 g in 1 CELLO PACK 2023-01-31 — Active
54340-0274-11 54340-274-11 4 CELLO PACK in 1 CARTON / 904 g in 1 CELLO PACK 2023-02-01 — Active
54340-0274-13 54340-274-13 12 CELLO PACK in 1 CARTON / 339 g in 1 CELLO PACK 2023-02-01 — Active
54340-0274-14 54340-274-14 8 CELLO PACK in 1 CARTON / 452 g in 1 CELLO PACK 2025-06-01 — Active

Pack size FAQ

What quantity is in this package?
This package contains 678 g — 678 g in 1 cello pack.
How does this package differ from NDC 54340-0274-01?
Both are Dial Antibacterial Bar .1 g/100g Soap — the drug itself is identical. This page's package is the 678 g one, while NDC 54340-0274-01 is the 180 g package.
What NDC number is used to bill for this package of Dial Antibacterial Bar .1 g/100g Soap?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Dial refresh and renew Antibacterial Mountain Fresh .1 g/100g 54340-0017-03 Henkel 3 packets — — FDA listed —
Dial Antibacterial with Vitamins .1 g/100g 54340-0020-01 Henkel 113 g — — FDA listed —
Dial refresh and renew Antibacterial white .1 g/100g 54340-0260-01 Henkel 113 g — — FDA listed —
Dial advanced clean Antibacterial gold .1 g/100g 54340-0262-01 Henkel 113 g — — FDA listed —
Dial Antibacterial Calm and Soothe .1 g/100g 54340-0266-03 Henkel 3 packets — — FDA listed —
Dial Antibacterial and Sensitive Aloe .1 g/100g 54340-0267-03 Henkel 16 cellos — — FDA listed —
Dial Complete Antibacterial Bar Spring Water .1 g/100g 54340-0270-08 Henkel 8 packets — — FDA listed —
Dial Antibacterial Bar .1 g/100g 54340-0272-20 Henkel 99 g — — FDA listed —
Dial Antibacterial Bar .1 g/100gthis 54340-0274-04 Henkel 678 g — — Discontinued —
Dial Antibacterial Bar .1 g/100g 54340-0278-04 Henkel 678 g — — Discontinued —
Dial antibacterial and sensitive hypoallergenic bar .1 g/100g 54340-0283-30 Henkel 1 cello — — FDA listed —
Dial Antibacterial Vitamin Bar .1 g/100g 54340-0286-02 Henkel 72 cellos — — FDA listed —
Dial refresh and renew Antibacterial Bar Spring Water .1 g/100g 54340-0300-01 Henkel 113 g — — FDA listed —
DK12 Oatmeal Antibacterial and Moisturizing .1 g/110g 62476-0104-15 Industria 140 g — — FDA listed —
DK12 Creamy Antibacterial and Moisturizing .1 g/110g 62476-0105-15 Industria 140 g — — FDA listed —
DK12 Fresh Energy Antibacterial and Moisturizing .1 g/110g 62476-0106-15 Industria 140 g — — FDA listed —
Escudo Ultra-Protect Original .1 g/100g 84529-0001-01 Indelpa, 115 g — — FDA listed —
Escudo Ultra-Protect Soft Care .1 g/100g 84529-0002-01 Indelpa, 115 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
Jul 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.

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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerHenkel Corporation
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code54340
First marketedJul 2017
Product typeHuman Otc Drug
Portfolio57 products on file

More NDCs from Henkel Corporation labeler code 54340

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 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 10 words ▾

Uses For washing to decrease the bacteria on the skin.

⏱️ Dosage and Administration 14 words ▾

Directions wet bar with water lather vigorously and wash skin rinse and dry thoroughly

⚠️ Warnings 32 words ▾

Warning For external use only. When using this product avoid contact with eyes. In case of eye contact, flush with water. Stop using and ask doctor if irritation or redness develops. Warnings

🧪 Active Ingredient 5 words ▾

Active Ingredient Benzalkonium Chloride 0.1%

🧪 Inactive Ingredients 50 words ▾

Inactive Ingredient Sodium Palmate Water Sodium Palm Kernelate Sodium Palmate Sodium Cocoate Glycerin Stearic Acid Palm Acid Palm Kernel Acid Coconut Acid Fragrance CI 77891 (Titanium Dioxide) Sodium Chloride Sorbitol Tetrasodium Glutamate Diacetate Alcohol CI 19140 (Yellow 5) CI 42053 (Green 3) CONTAINS ONE OR MORE OF THESE INGREDIENTS Ingredients

🎯 Purpose 2 words ▾

Purpose Antibacterial

📄 Keep Out of Reach of Children 19 words ▾

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

📄 Package Label / Principal Display Panel 6 words ▾

4 pck MF PDP MF DFB

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 Dial Antibacterial Bar (this brand).

Top reported reactions

Application Site Pruritus1
Application Site Rash1
Insomnia1
Pain1

Reporter sex

1 reports
Reports over time (by year) — tap or hover for the count & year
2020 2022 2024 2026 1 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.

About this NDC listing & data coverage

Over-the-counter (OTC) product No longer marketed (per FDA listing data)
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) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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.
Does this product come in other package sizes?
Yes — the FDA directory lists 12 other package presentations of this same product, including 4 cellos (54340-0274-11), 8 cellos (54340-0274-14), 12 cellos (54340-0274-13). 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?
Henkel Corporation 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.
← 54340-0272-20 · Henkel 54340-0278-04 · Henkel →
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.