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AFCO 5508 Sanifect Foam-E II Chloroxylenol 2081980 mg/208198mL Liquid, 3785 mL — NDC 66949-0141-03 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

AFCO 5508 Sanifect Foam-E II Chloroxylenol 2081980 mg/208198mL Liquid, 3785 mL — NDC 66949-141-03 (Billing 66949-0141-03)

by Zep Inc. · 3785 mL in 1 CASE

This is a package of 3,785 mL of AFCO 5508 Sanifect Foam-E II Chloroxylenol 2081980 mg/208198mL Liquid from Zep Inc., marketed since Oct 2025 and currently FDA-listed.

NDC 66949-0141-03
🏷️ FDA NDC (as labeled) 66949-141-03 billing pads the product segment with a zero
This package
Contains3785 mL Pack sizes3 compare ↓
Product page 66949-0141-01 Also comes in: 6000 ml 66949-141-02 208198 ml 66949-141-01
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 66949-141-03 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
66949 labeler · 141 product · 03 package
Package marketed since
Oct 23, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 6694914103 8
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 66949-141-03
Product NDC 66949-141
11-digit billing NDC 66949014103
RxCUI 413257
UNII 0F32U78V2Q
Application # 505G(a)(3)
SPL Set ID 46deac5c-97e8-8924-e063-6294a90a5dbc
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-10-23
Route TOPICAL
Dosage form LIQUID
Substance CHLOROXYLENOL
Quick answers
  • RxCUI (RxNorm): 413257
Why two NDCs? The FDA registers this code as 66949-141-03 — 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 → 66949-0141-03. 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?

Afco 5508 Sanifect Foam-E II is a liquid topical foam product that contains chloroxylenol, an antimicrobial ingredient commonly used in skin-cleansing products. Chloroxylenol is typically included in soaps and sanitizing preparations intended to reduce bacteria on the skin surface. This product is an over-the-counter monograph drug, meaning it is marketed under FDA's established guidelines for antiseptic and germicidal skin cleansers rather than as an individually approved application.

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 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: 6000 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
66949-0141-01 66949-141-01 Main listing 208198 mL in 1 DRUM 2025-10-23 — Active
66949-0141-02 66949-141-02 6000 mL in 1 CASE 2025-10-23 — Active
66949-0141-03 You're viewing this 3785 mL in 1 CASE 2025-10-23 — Active

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

Pack size FAQ

What quantity is in this package?
This package contains 3785 mL — 3785 ml in 1 case.
How does this package differ from NDC 66949-0141-02?
Both are AFCO 5508 Sanifect Foam-E II Chloroxylenol 2081980 mg/208198mL Liquid — the drug itself is identical. This page's package is the 3785 mL one, while NDC 66949-0141-02 is the 6000 ml package.
What NDC number is used to bill for this package of AFCO 5508 Sanifect Foam-E II Chloroxylenol 2081980 mg/208198mL 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
Kindest Kare Hand Antimicrobial Handwash 1 g/100mL 11084-0036-41 SC 1000 ml — — FDA listed —
Acute-Kare Healthcare Personnel Handwash 1 g/100mL 11084-0800-41 SC 1000 ml — — FDA listed —
DigiClean E 1 mg/100mL 47593-0308-41 Ecolab 750 ml — — FDA listed —
Ecolab 10 mg/mL 47593-0506-41 Ecolab 750 ml — — FDA listed —
VioNexus 1 g/100mL 55443-0600-03 Metrex 2 bottles — — FDA listed —
SoftenSure Foam Antimicrobial 10 mg/mL 59900-0127-05 Best 1250 ml — — FDA listed —
Soften Sure Foam Antimicrobial 10 g/1000mL 59900-0211-06 Best 1000 ml — — FDA listed —
Prestige 10 mg/mL 63621-0335-14 Sunburst 3785 ml — — FDA listed —
FoamyIQ Healthcare Personnel Handwash 10.11 g/L 64009-0203-06 Spartan 1.25 l — — FDA listed —
Lite nFoamy Healthcare Personnel Handwash 10.11 g/L 64009-0335-82 Spartan 532 l — — FDA listed —
Antiseptic Hand Cleaner 10.11 g/L 64009-0336-85 Spartan 3.79 l — — FDA listed —
Clean Xpress Antiseptic Hand Cleaner 10 mg/mL 64009-0338-02 Spartan 1000 ml — — FDA listed —
Soft Care Defend Foam Antibacterial Handwash 1 g/100mL 64536-8308-02 Diversey, 1200 ml — — Discontinued —
Soft Care Defend Antibacterial Handwash 1 g/100mL 64536-8748-02 Diversey, 1200 ml — — Discontinued —
Soft Care Defend Antibacterial Handwash 10 g/L 64536-8760-02 Diversey, 3.78 l — — FDA listed —
WhiskCare 365 10 mg/mL 65585-0365-02 Whisk 3785 ml — — FDA listed —
AFCO 5508 Sanifect Foam-E II 2081980 mg/208198mL 66949-0139-01 Zep 208198 ml — — FDA listed —
AFCO 5508 Sanifect Foam-E II 2081980 mg/208198mLthis 66949-0141-03 Zep 3785 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

🏛️
2025
On the market since
Oct 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 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • UNII Q7AO2R1M0B
    Ammonium lauryl sulfate is a mild detergent and foaming agent derived from plant oils. It helps mix water and oil-based ingredients together and creates a light foam in topical formulations like shampoos and cleansers.
  • 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 C80684146D
    A foaming agent and thickener derived from coconut oil. It helps create a smooth texture and stable foam in liquid or semi-solid medicines, improving how the product feels and applies.
  • UNII 62V75NI93W
    A surfactant derived from coconut oil that helps cleanse and remove oils from skin or hair. In medicines and personal care products, it acts as a cleanser and foaming agent.
  • UNII 7FLD91C86K
    Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life and consistency.
  • 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 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII 632GS99618
    Sodium lauroyl sarcosinate is a mild, plant-derived cleaning agent used in medicines as a surfactant and emulsifier. It helps mix oil and water-based ingredients and may aid tablet disintegration.
  • UNII 3P5SU53360
    Triethylene glycol is a synthetic liquid that acts as a solvent and humectant in medicines. It helps dissolve active ingredients and keeps liquid formulations from drying out.
  • 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.

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

The official label also statesWater, Ammonium Lauryl Sulfate, Ethanol, Sodium Lauroyl Sarcosinate, Triethylene Glycol, Propylene Glycol, Glycerin, Disodium EDTA, Cocomidopropyl Hydroxysultaine, Citric Acid, Cocamide MIPA.

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

LabelerZep Inc.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code66949
First marketedOct 2025
Product typeHuman Otc Drug
Portfolio28 products on file

More NDCs from Zep Inc. labeler code 66949

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 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 13 words ▾

Uses For handwashing to decrease bacteria on the skin. Recommended for repeated use.

⏱️ Dosage and Administration 31 words ▾

Directions Wet hands with water, apply enough product to cover all hand surfaces, rub hands together for at least 30 seconds to work into lather. Rinse thoroughly and dry hands completely.

⚠️ Warnings 5 words ▾

Warnings FOR EXTERNAL USE ONLY

🧪 Active Ingredient 5 words ▾

Active ingredient Chloroxylenol 1.0% w/w

🧪 Inactive Ingredients 23 words ▾

Inactive ingredients Water, Ammonium Lauryl Sulfate, Ethanol, Sodium Lauroyl Sarcosinate, Triethylene Glycol, Propylene Glycol, Glycerin, Disodium EDTA, Cocomidopropyl Hydroxysultaine, Citric Acid, Cocamide MIPA.

🎯 Purpose 2 words ▾

Purpose Antibacterial

📄 When Using This Product 20 words ▾

When using this product When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

📄 Stop Use and Ask a Doctor If 20 words ▾

Stop use and ask a doctor Stop use and ask a doctor if if irritation or redness develops and persists.

📄 Keep Out of Reach of Children 23 words ▾

Keep out of reach of children Keep out of reach of children. If swallowed, get medical help or contact poison control center immediately.

📄 Other Information 11 words ▾

Other information For Food Processing, Food Service and Professional Use Only.

📄 Questions or Comments 28 words ▾

Questions or comments? For product or technical information, contact ZEP, INC. Monday to Friday 8 AM to 4 PM EST at 1-877-428-9937 or visit our website at www.zep.com.

📄 Package Label / Principal Display Panel 2 words ▾

139 AF5508

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) ✓ 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 2 other package presentations of this same product, including 6000 ml (66949-0141-02), 208198 ml (66949-0141-01). 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.
← 66949-0140-01 · Zep 66949-0387-04 · Zep →
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.