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E2 hand wash E2 Sanitizing Hand Soap .13 mg/100mL Soap, 3785.4 mL — NDC 74683-6300-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

E2 hand wash E2 Sanitizing Hand Soap .13 mg/100mL Soap, 3785.4 mL — NDC 74683-6300-1 (Billing 74683-6300-01)

by Horizon Tool Inc. · 3785.4 mL in 1 BOTTLE, PLASTIC

This is a package of 3,785.4 mL of E2 hand wash E2 Sanitizing Hand Soap .13 mg/100mL Soap from Horizon Tool Inc., marketed since May 2025 and currently FDA-listed. It is this product's only package size.

NDC 74683-6300-01
🏷️ FDA NDC (as labeled) 74683-6300-1 billing pads the package segment with a zero
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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 74683-6300-1
Product NDC 74683-6300
11-digit billing NDC 74683630001
RxCUI 581662, 1241663, 1489307, 2286987
UNII F5UM2KM3W7
UPC 0047084226162, 0047084022542, 0047084022580, 0047084226285 +2 more
Application # M016
SPL Set ID a40afa46-a07d-f864-e053-2a95a90aef8a
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-05-01
Route TOPICAL
Dosage form SOAP
Substance BENZALKONIUM CHLORIDE
Quick answers
  • RxCUI (RxNorm): 581662
Why two NDCs? The FDA registers this code as 74683-6300-1 — a 5-4-1 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 package segment → 74683-6300-01. 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 Other antiseptics and disinfectants class.

Drug family (ATC) Other antiseptics and disinfectants, Antidotes, Nerve depressants
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?

E2 Sanitizing Hand Soap is a topical soap product containing benzalkonium chloride as its active ingredient. Benzalkonium chloride is an antimicrobial agent typically used in hand-washing products to help reduce bacteria and germs on the skin. This product is marketed as an over-the-counter monograph drug, meaning it is formulated according to FDA established guidelines for antiseptic hand soaps 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 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.
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
74683-6300-01 You're viewing this Main listing 3785.4 mL in 1 BOTTLE, PLASTIC 2025-05-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
E2 hand wash .13 mg/100mLthis 74683-6300-01 Horizon 3785.4 ml — — FDA listed —
E2 Hand Wash .13 mg/100mL 74683-6401-01 Horizon 3785.4 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
May 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 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.
  • 6 mL / 100 mL UNII 5OCF3O11KX
    A plant-derived surfactant made from coconut oil. It helps mix oil and water ingredients together in the formulation and can improve how the medicine spreads or feels on the skin.
  • 1.5 mL / 100 mL UNII Z17H97EA6Y
    A plant-derived mild cleanser made from natural sugars and oils. It acts as an emulsifier and surfactant to help mix water and oil-based ingredients together in the medicine.
  • 2 mL / 100 mL 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.
  • 0.8 mL / 100 mL UNII T4V6TWG28D
    A plant-derived thickening agent made from cellulose. It increases viscosity and helps form a gel or paste consistency in medications, and may serve as a binder or coating material in various formulations.
  • 0.75 mL / 100 mL UNII 15O9QS218W
    A chemical preservative that prevents mold, bacteria, and yeast from growing in liquid medicines and personal care products. It keeps the product safe and effective throughout its shelf life.
  • 88.69 mL / 100 mL 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.

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

The official label also statesglycerin, hydrogen peroxide, purified water USP

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

LabelerHorizon Tool Inc.
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code74683
First marketedMay 2025
Product typeHuman Otc Drug
Portfolio2 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 ⏱️ Dosage and Administration ⚠️ Warnings 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 21 words ▾

Use Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

⏱️ Dosage and Administration 29 words ▾

Directions Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

⚠️ Warnings 12 words ▾

Warnings For external use only. Flammable. Keep away from heat or flame

📦 Storage and Handling 14 words ▾

Other information Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

🧪 Active Ingredient 7 words ▾

Active Ingredient(s) Alcohol 80% v/v. Purpose: Antiseptic

🧪 Inactive Ingredients 8 words ▾

Inactive ingredients glycerin, hydrogen peroxide, purified water USP

🎯 Purpose 4 words ▾

Purpose Antiseptic, Hand Sanitizer

📄 Do Not Use 15 words ▾

Do not use in children less than 2 months of age on open skin wounds

📄 When Using This Product 60 words ▾

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Stop Use and Ask a Doctor If 19 words ▾

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

📄 Keep Out of Reach of Children 19 words ▾

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

📄 Package Label / Principal Display Panel ~2 min read ▾

Package Label - Principal Display Panel 3785.4 mL NDC: 74683-6401-1 3785.5 mL NDC: 74683-6400-1 3785.4 mL NDC: 74683-6300-1 3785.41 mL NDC: 74683-2001-2 473 mL NDC: 74683-2001-1 118 mL NDC: 74683-5001-4 250 mL NDC: 74683-5001-3 59 mL NDC: 74683-5001-2 473 mL NDC: 74683-5001-1 250 mL NDC: 74683-1002-1 3785.4 mL NDC: 74683-6200-3 250 mL NDC: 7463-6200-2 3785.4 mL NDC: 74683-6200-1 3785.4 mL NDC: 74683-6000-1 59 mL NDC: 74683-2100-1 946.35 mL NDC: 74683-3001-1 262 mL NDC: 74683-2500-1 1892.71 mL NDC: 74683-5000-9 208.2 L NDC: 74683-5000-8 946.35 mL NDC: 74683-5000-7 946.35 mL NDC: 74683-5000-7 473 mL NDC: 74683-5000-6 3785.41 mL NDC: 74683-5000-5 3785.41 mL NDC: 74683-5000-4 354.8 mL NDC: 74683-5000-3 236 mL NDC: 74683-5000-2 118 mL NDC: 74683-5000-1 118 mL NDC: 74683-4000-1 3 mL NDC 74683-3000-8 3 mL NDC 74683-3000-8 3 mL NDC 74683-3000-9 3 mL NDC 74683-3000-9 3785.41 mL NDC 74683-3000-7 3785.41 mL NDC 74683-3000-6 3785.41 mL NDC 74683-3000-5 1892.71 mL NDC 74683-3000-4 946.35 mL NDC 74683-3000-3 946.35 mL NDC 74683-3000-3 118 mL NDC 74683-3000-2 59 mL NDC 74683-3000-1 59 mL NDC 74683-3000-1 473 mL NDC 74683-1000-9 236 mL NDC 74683-1000-8 059 mL NDC: 74683-1000-6 059 mL NDC: 74683-1000-6 74683-1000-7 236 mL NDC: 74683-2000-1 473 mL NDC: 74683-1000-2 946.35 mL NDC: 74683-1000-3 946.35 mL NDC: 74683-1000-3 1892.71 mL NDC: 74683-1000-4 3785.41 mL NDC: 74683-1000-5 473 mL NDC: 74683-2000-1 473 mL NDC: 74683-2000-1 946.35 mL NDC: 74683-2000-2 946.35 mL NDC: 74683-2000-2 1892.71 mL NDC: 74683-2000-3 3785.41 mL NDC: 74683-2000-4 3785.4 mL label 3785.4 mL label 3785.41 mL label 473 mL front label 473 mL rear label 118 mL label 250 mL label 59mL Label 473 mL label 250 mL label 3785.4 mL label 250 mL label 3785.4 mL label 3785.4 mL label 59ml label 946.35 ml label 262 mL wipe label 1892.71 mL label 208.2 L label 946.35 mL rear label 946.35 mL front label 473 mL label 3785.41 mL 4cc label 3785.41 mL 10cc label 354.8 mL label 236 mL label 118 mL label 118 mL Tiger gel label 3mL gel rear 3mL gel front 3mL gel rear 3mL gel front 3785.41mL gel 3785.41mL gel 3785.41mL gel 1892.71mL gel 946.35mL gel rear 946.35mL gel front 118mL gel 59mL gel rear 59mL gel front 473mL gel TenSan 236mL gel TenSan 59 mL gel front 59 mL gel rear 118 mL gel 236mL gel 473mL gel 946.35 mL front label 946.35mL gel rear 1892.71mL gel 3785.41mL gel 473mL liquid front 473mL liquid rear 946.35mL liquid front 946.35mL liquid rear 1892.71mL liquid 3785.41mL liquid

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 Horizon Tool Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Horizon Tool 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.
← 74680-0231-75 · Unico 74683-6401-01 · Horizon →
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.