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Alpet E2 Sanitizing Foam Chloroxylenol 15 g/1000mL Soap, 208175 mL — NDC 59900-0208-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Alpet E2 Sanitizing Foam Chloroxylenol 15 g/1000mL Soap, 208175 mL — NDC 59900-208-02 (Billing 59900-0208-02)

by Best Sanitizers, Inc. · 208175 mL in 1 DRUM

This is a package of 208,175 mL of Alpet E2 Sanitizing Foam Chloroxylenol 15 g/1000mL Soap from Best Sanitizers, Inc., marketed since Feb 2008 and currently FDA-listed.

NDC 59900-0208-02
🏷️ FDA NDC (as labeled) 59900-208-02 billing pads the product segment with a zero
This package
Contains208175 mL Pack sizes9 compare ↓
Product page 59900-0208-01 Also comes in: 59 ml 59900-208-08 118 ml 59900-208-05 500 ml 59900-208-03 1000 ml 59900-208-04 1000 ml 59900-208-06 2000 ml 59900-208-07 3785 ml 59900-208-01 946250 ml 59900-208-09
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 →

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 59900-208-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
59900 labeler · 208 product · 02 package
Package marketed since
Feb 1, 2008
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 5990020802 4
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 59900-208-02
Product NDC 59900-208
11-digit billing NDC 59900020802
RxCUI 1043129
UNII 0F32U78V2Q
Application # 505G(a)(3)
SPL Set ID 5c7bdeb0-25e3-4e7a-8789-6b6fc6f32a31
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2008-02-01
Route TOPICAL
Dosage form SOAP
Substance CHLOROXYLENOL
Quick answers
  • RxCUI (RxNorm): 1043129
Why two NDCs? The FDA registers this code as 59900-208-02 — 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 → 59900-0208-02. 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?

Alpet E2 Sanitizing Foam is an over-the-counter topical soap containing chloroxylenol, an antimicrobial ingredient commonly used in hand-cleaning and skin-sanitizing products. The product is marketed as an OTC monograph drug, meaning it follows FDA's established safety and effectiveness rules for this category of sanitizing soaps rather than undergoing individual product review. Chloroxylenol is typically included in sanitizing formulations for its antimicrobial properties.

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: 59 ml 118 ml 500 ml 1000 ml 1000 ml 2000 ml 3785 ml 946250 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
59900-0208-01 59900-208-01 Main listing 3785 mL in 1 BOTTLE, PLASTIC 2008-02-01 — Active
59900-0208-02 You're viewing this 208175 mL in 1 DRUM 2008-02-01 — Active
59900-0208-03 59900-208-03 500 mL in 1 BOTTLE, PLASTIC 2008-02-01 — Active
59900-0208-04 59900-208-04 1000 mL in 1 BAG 2008-02-01 — Active
59900-0208-05 59900-208-05 118 mL in 1 BOTTLE, PLASTIC 2008-02-01 — Active
59900-0208-06 59900-208-06 1000 mL in 1 BOTTLE, PLASTIC 2008-02-01 — Active
59900-0208-07 59900-208-07 2000 mL in 1 BOTTLE, PLASTIC 2008-02-01 — Active
59900-0208-08 59900-208-08 59 mL in 1 BOTTLE, PLASTIC 2008-02-01 — Active
59900-0208-09 59900-208-09 946250 mL in 1 DRUM 2008-02-01 — Active

Pack size FAQ

What quantity is in this package?
This package contains 208175 mL — 208175 ml in 1 drum.
How does this package differ from NDC 59900-0208-08?
Both are Alpet E2 Sanitizing Foam Chloroxylenol 15 g/1000mL Soap — the drug itself is identical. This page's package is the 208175 mL one, while NDC 59900-0208-08 is the 59 ml package.
What NDC number is used to bill for this package of Alpet E2 Sanitizing Foam Chloroxylenol 15 g/1000mL 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
Alpet E2 Sanitizing Foam 15 g/1000mLthis 59900-0208-02 Best 208175 ml — — FDA listed —
Chemstation E2 15 g/L 71212-0103-00 Chemstation 208.198 l — — 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

🏛️
2008
On the market since
Feb 2008
📍
2026
Currently FDA-listed
18 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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • 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 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 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 ND2M416302
    Isopropyl alcohol is a clear liquid solvent derived from petroleum. In medicines, it dissolves active ingredients and other components, helps the product flow smoothly, and aids in sterilization during manufacturing.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII BPV390UAP0
    Sodium laureth sulfate is a mild detergent and surfactant derived from coconut oil or petroleum. It helps mix oil and water in formulations and is often used as a cleaning or foaming agent in topical products like shampoos and cleansers.
  • UNII 4NM5039Y5X
    Triclosan is an antimicrobial agent added to medicines to prevent bacterial and fungal growth, helping preserve the product's shelf life and maintain sterility during storage and use.
  • 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.

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

The official label also statesWater, Sodium Laureth Sulfate, Isopropyl alcohol, Phenoxyethanol, Glycerine, Triclosan, TetraSodium EDTA, Citric Acid

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

LabelerBest Sanitizers, Inc.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code59900
First marketedFeb 2008
Product typeHuman Otc Drug
Portfolio14 products on file

More NDCs from Best Sanitizers, Inc. labeler code 59900

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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 17 words ▾

Uses Helps reduce bacteria that potentially can cause diseases Helps to prevent cross contamination by hand contact

⏱️ Dosage and Administration 39 words ▾

Directions Apply cleaner to palm of hand Lather and scrub hands (including fingers, wrist, and cuticles) vigorously for 30 seconds Rinse with water until all cleaner is removed from hands Dry completely (incomplete drying may lead to happed skin)

⚠️ Warnings 5 words ▾

Warnings For external use only

📦 Storage and Handling 11 words ▾

Other information Store in a cool dry place below 104° F

🧪 Active Ingredient 5 words ▾

Active Ingredient Chloroxylenol 1.5% w/w

🧪 Inactive Ingredients 15 words ▾

Inactive ingredients Water, Sodium Laureth Sulfate, Isopropyl alcohol, Phenoxyethanol, Glycerine, Triclosan, TetraSodium EDTA, Citric Acid

🎯 Purpose 4 words ▾

Purpose Antiseptic Hand Cleanser

📄 Keep Out of Reach of Children 70 words ▾

Keep out of reach of children. In case of eye contact, flush with water for 15 minutes, if irritation persists, get medical attention. In case of accidental ingestion, seek medical attention or contact a poison control center immediately. This product must be dispensed from an adequate dispenser located a sufficient distance from processing line to prevent accidental product contamination. Do not contaminate water, food or feed by storage and disposal.

📄 Questions or Comments 11 words ▾

Questions? Contact Best Sanitizers Mon-Fri 9am - 4p PST at 888-225-3267

📄 Package Label / Principal Display Panel 30 words ▾

NDC: 59900-208-01 NDC: 59900-208-02 NDC: 59900-208-03 NDC: 59900-208-04 NDC: 59900-208-05 NDC: 59900-208-06 NDC: 59900-208-07 NDC: 59900-208-08 NDC: 59900-208-09 Alpet E2 Sanitizing Foam Soap For Food Industry Professionals Principal Display Panel

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 Best Sanitizers, 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 8 other package presentations of this same product, including 59 ml (59900-0208-08), 118 ml (59900-0208-05), 500 ml (59900-0208-03). 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?
Best Sanitizers, 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.
← 59900-0130-01 · Best 59900-0211-06 · Best →
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.