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Zep E-2 Hand Sanitizing Cleaner Chloroxylenol 3 g/100mL Liquid, 6000 mL — NDC 66949-0125-06 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Zep E-2 Hand Sanitizing Cleaner Chloroxylenol 3 g/100mL Liquid, 6000 mL — NDC 66949-125-06 (Billing 66949-0125-06)

by Zep Inc. · 6000 mL in 1 CASE

This is a package of 6,000 mL of Zep E-2 Hand Sanitizing Cleaner Chloroxylenol 3 g/100mL Liquid from Zep Inc., marketed since Jun 1988 and currently FDA-listed.

NDC 66949-0125-06
🏷️ FDA NDC (as labeled) 66949-125-06 billing pads the product segment with a zero
This package
Contains6000 mL Pack sizes5 compare ↓
OTC On market Non-controlled ⇄ 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 →

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 66949-125-06
Product NDC 66949-125
11-digit billing NDC 66949012506
RxCUI 413259
UNII 0F32U78V2Q
Application # 505G(a)(3)
SPL Set ID b43e4f86-44dd-3842-e053-2a95a90ab41d
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 1988-06-15
Route TOPICAL
Dosage form LIQUID
Substance CHLOROXYLENOL
Quick answers
  • RxCUI (RxNorm): 413259
Why two NDCs? The FDA registers this code as 66949-125-06 — 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 → 66949-0125-06. 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.

RxNorm drug class

This medicine belongs to the Phenol and derivatives class.

Drug family (ATC) Phenol and derivatives
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?

Zep E-2 Hand Sanitizing Cleaner is a topical liquid hand sanitizer containing chloroxylenol, an antimicrobial agent. Chloroxylenol is commonly used in over-the-counter hand sanitizers and cleaning products to help reduce bacteria and germs on the skin. This product is marketed as an OTC monograph drug, meaning it is manufactured under FDA's established rules for hand sanitizer products rather than as an individually reviewed application. It is applied directly to the hands for cleansing purposes.

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 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.
Try another pack size: 3875 ml 11400 ml 15140 ml 208198 ml
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
66949-0125-01 66949-125-01 Main listing 11400 mL in 1 CASE 1988-06-15 — Active
66949-0125-06 You're viewing this 6000 mL in 1 CASE 1988-06-15 — Active
66949-0125-24 66949-125-24 15140 mL in 1 CASE 1988-06-15 — Active
66949-0125-85 66949-125-85 208198 mL in 1 DRUM 1988-06-15 — Active
66949-0125-04 66949-125-04 3875 mL in 1 CASE 1988-06-15 — Active

You're viewing one of 5 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 6000 mL — 6000 ml in 1 case.
How does this package differ from NDC 66949-0125-04?
Both are Zep E-2 Hand Sanitizing Cleaner Chloroxylenol 3 g/100mL Liquid — the drug itself is identical. This page's package is the 6000 mL one, while NDC 66949-0125-04 is the 3875 ml package.
What NDC number is used to bill for this package of Zep E-2 Hand Sanitizing Cleaner Chloroxylenol 3 g/100mL Liquid?
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
Bd E-Z Scrub 30 mg/mL 17271-0116-03 Becton 16 ml — — FDA listed —
Recovery Antiseptic Skin Prep 3 g/100mL 49436-0377-30 PURKLENZ 900 ml — — FDA listed —
Zep E-2 Hand Sanitizing Cleaner 3 g/100mLthis 66949-0125-06 Zep 6000 ml — — 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

🏛️
1988
On the market since
Jun 1988
📍
2026
Currently FDA-listed
38 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

LabelerZep Inc.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code66949
First marketedJun 1988
Product typeHuman Otc Drug
Portfolio28 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.

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 8 words ▾

Uses Hand washing to decrease bacteria on skin

⏱️ Dosage and Administration 31 words ▾

Directions Wet hands with water. Place hands under dispenser and apply liquid soap. Massage soap into hands and wrists, emphasizing back of hands, knuckles and cuticles. Rinse hands thoroughly and dry.

⚠️ Warnings 5 words ▾

Warnings For external use only.

🧪 Active Ingredient 4 words ▾

Active ingredient Chloroxylenol 3.0%

🧪 Inactive Ingredients 19 words ▾

Inactive ingredients Water, Sodium C14-16 Olefin Sulfonate, Triethylene Glycol, Cocamidopropyl Hydroxysultaine, Hydroxyethyl Cellulose, PEG-75 Lanolin, Methylchloroisothiazolinone, Methylisothiazolinone, Citric Acid

🎯 Purpose 4 words ▾

Purpose Antiseptic Hand Wash

📄 Do Not Use 11 words ▾

Do not use Do not use in or around the eyes.

📄 When Using This Product 66 words ▾

When using this product If eye contact occurs, rinse promptly and thoroughly with water. Do not swallow. If swallowed, do not induce vomiting and if individual is conscious, give large quantities of water to drink and consult a physician immediately. Allergy alert: May cause skin reactions. Symptoms may include: skin reddening, blisters, rash If a skin reaction occurs, stop use and seek medical help right away

📄 Stop Use and Ask a Doctor If 23 words ▾

Stop use and ask a doctor Stop use and ask a doctor if skin irritation or redness persists for more than 72 hours.

📄 Keep Out of Reach of Children 25 words ▾

Keep out of reach of children and pets Keep out of reach of children and pets. Children must be supervised in use of this product.

📄 Other Information 20 words ▾

Other information Store at room temperature. Do not freeze. Dispose in accordance with all applicable federal, state and local regulations.

📄 Questions or Comments 6 words ▾

Questions of comments? Call 1-877-I-BUY_ZEP (1-877-428-9937)

📄 Package Label / Principal Display Panel 1 words ▾

125_0920

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

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) — 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.
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 Zep Inc.. 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 4 other package presentations of this same product, including 3875 ml (66949-0125-04), 11400 ml (66949-0125-01), 15140 ml (66949-0125-24). 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?
Zep Inc. 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.
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.