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DK12 Fresh Energy Antibacterial and Moisturizing Benzalkonium Chloride 0.1% .1 g/110g Soap, 420 g

by Industria La Popular, S.A. · 420 g in 1 CELLO PACK (62476-106-42)
NDC 62476-0106-42
🏷️ FDA NDC (as labeled) 62476-106-42 billing pads the product segment with a zero
This package
Contains420 g Pack sizes2 compare ↓
Also comes in: 140 g 62476-0106-15
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) 62476-106-42
Product NDC 62476-106
11-digit billing NDC 62476010642
RxCUI 1926450
UNII F5UM2KM3W7
Application # M003
SPL Set ID fe80635d-9594-abf3-e053-6394a90aa78b
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-06-01
Route TOPICAL
Dosage form SOAP
Substance BENZALKONIUM CHLORIDE
Why two NDCs? The FDA registers this code as 62476-106-42 — 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 → 62476-0106-42. 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

LabelerIndustria La Popular, S.A.
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code62476
First marketedJun 2023
Product typeHuman Otc Drug
Portfolio16 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?

DK12 Fresh Energy is a topical antibacterial soap containing benzalkonium chloride 0.1% as its active ingredient. Benzalkonium chloride is a type of antimicrobial agent typically used in over-the-counter soaps to help reduce bacteria on the skin. This is an OTC monograph product, meaning it is marketed under FDA's established rules for antibacterial soap products rather than as an individually approved application. The soap is intended for routine cleansing and is applied topically to the skin.

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.

  • UNII 0C9AC7D6XU
    A plant-derived fat from shea nut kernels that remains after soap-making. It acts as a moisturizer, emollient, and texture enhancer in topical formulations, helping soften skin and improve product spreadability.
  • UNII Q9L0O73W7L
    Coconut oil is a natural fat extracted from coconut fruit. It's used in medicines as a lubricant, emollient, or carrier to help dissolve or deliver active ingredients smoothly through the formulation.
  • 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 H3R47K3TBD
    FD&C Blue No. 1 is a synthetic blue dye approved for use in foods and medicines. It serves as a colorant to give the medication its distinctive appearance and help with product identification.
  • 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 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 285CYO341L
    Sodium polyacrylate is a synthetic polymer that absorbs and holds water. In medicines, it acts as a disintegrant, helping tablets break apart quickly in the stomach, and as a binder, holding tablet ingredients together.
  • UNII O8232NY3SJ
    A plant-based carbohydrate derived from corn kernels. It acts as a filler to add bulk, a binder to hold ingredients together, and a disintegrant to help the tablet break apart in your stomach for absorption.
  • 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.

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

The official label also statesSodium Palm Kernelate, Water, Glycerin, Fragrance (Perfume), Sodium Polyacrylate, Zea May Starch, Butyrospermum Parkii (Shea Butter), Etidronic Acid, Titanium Dioxide, Cocos Nucitera (coconut) oil, FD&C Blue No. 1.

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: 140 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
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/100g 54340-0274-01 Henkel 180 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/110gthis 62476-0106-42 Industria 420 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 —
DK12 Vitamin E Antibacterial and Moisturizing .1 g/110g 62476-0107-15 Industria 140 g — — FDA listed —
Olimpo Antibacterial .1 g/110g 62476-0108-01 Industria 100 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

🏛️
2023
On the market since
Jun 2023
📍
2026
Currently FDA-listed
3 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 DK12 Fresh Energy Antibacterial and Moisturizing (this brand).

Top reported reactions

Application Site Burn1
Application Site Vesicles1
Chemical Burn1
Product Complaint1

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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
62476-0106-15 140 g in 1 CELLO PACK (62476-106-15) 2023-06-01 Active
62476-0106-42 You're viewing this 420 g in 1 CELLO PACK (62476-106-42) 2023-06-01 Active

You're viewing the largest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 62476-0106-42?
NDC 62476-0106-42 contains 420 g — 420 g in 1 cello pack.
What is the difference between NDC 62476-0106-42 and NDC 62476-0106-15?
Both are DK12 Fresh Energy Antibacterial and Moisturizing Benzalkonium Chloride 0.1% .1 g/110g Soap — the drug itself is identical. NDC 62476-0106-42 is the 420 g package, while NDC 62476-0106-15 is the 140 g package.
What NDC number is used to bill for this package of DK12 Fresh Energy Antibacterial and Moisturizing Benzalkonium Chloride 0.1% .1 g/110g Soap?
Bill NDC 62476-0106-42 — the 11-digit billing format is 62476010642. 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 — 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 62476-106-42, 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: 62476-0106-42, written without dashes as 62476010642. 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 62476-0106-42, the first segment (62476) is the labeler code FDA assigned to Industria La Popular, S.A.; the middle segment (0106) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (42) 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 Industria La Popular, S.A.. 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 1 other package presentation of this same product, including 140 g (62476-0106-15). 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?
Industria La Popular, S.A. 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 washing to decrease bacteria on the skin.

⏱️ Dosage and Administration 14 words ▾

Directions Wet bar with water Lather vigorously and wash skin Rinse and dry thoroughly

⚠️ Warnings 5 words ▾

Warnings For External Use only.

🧪 Active Ingredient 5 words ▾

Active Ingredient Benzalkonium Chloride 0.1%

🧪 Inactive Ingredients 30 words ▾

Inactive Ingredients Sodium Palm Kernelate, Water, Glycerin, Fragrance (Perfume), Sodium Polyacrylate, Zea May Starch, Butyrospermum Parkii (Shea Butter), Etidronic Acid, Titanium Dioxide, Cocos Nucitera (coconut) oil, FD&C Blue No. 1.

🎯 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 ↗
← 62476-0105-15 · Industria 62476-0107-15 · Industria →
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.