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Hillyard Citrus Fresh Antimicrobial Foaming Chloroxylenol .5 g/100mL Liquid, 2000 mL — NDC 76402-0408-12 package photo

Hillyard Citrus Fresh Antimicrobial Foaming Chloroxylenol .5 g/100mL Liquid, 2000 mL

by Hillyard GMP · 2000 mL in 1 BOTTLE, PLASTIC (76402-408-12)
NDC 76402-0408-12
🏷️ FDA NDC (as labeled) 76402-408-12 billing pads the product segment with a zero
This package
Contains2000 mL Pack sizes5 compare ↓
Also comes in: 414 ml 76402-0408-82 1000 ml 76402-0408-02 1250 ml 76402-0408-03 3785 ml 76402-0408-06
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) 76402-408-12
Product NDC 76402-408
11-digit billing NDC 76402040812
RxCUI 436367
UNII 0F32U78V2Q
Application # 505G(a)(3)
SPL Set ID d2b2581d-0e45-4b4d-8610-248bf9d2bf75
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2015-09-01
Route TOPICAL
Dosage form LIQUID
Substance CHLOROXYLENOL
Why two NDCs? The FDA registers this code as 76402-408-12 — 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 → 76402-0408-12. 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.

🏭 Manufacturer & labeler

LabelerHillyard GMP
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code76402
First marketedSep 2015
Product typeHuman Otc Drug
Portfolio8 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?

Hillyard Citrus Fresh is a foaming liquid antimicrobial soap marketed as an over-the-counter monograph product for topical use on the skin. It contains chloroxylenol, a germicidal ingredient commonly found in antimicrobial hand soaps and cleansers. Chloroxylenol is typically used to reduce bacteria and other microorganisms on the skin surface. This product is intended as a general-purpose antimicrobial cleanser.

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 5KV86114PT
    A chemical compound used in medicines as a pH buffer and neutralizing agent. It helps maintain the proper acidity level in liquid formulations to improve stability and make the medicine easier to take.
  • 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 XF417D3PSL
    Anhydrous citric acid is a sour, crystalline powder derived from citric acid with water removed. In medicines, it acts as a buffer to control pH, adds tartness to improve taste, and helps tablets disintegrate.
  • UNII LKG8494WBH
    Benzyl alcohol is a clear liquid used as a preservative and solvent in medicines. It helps prevent bacterial and fungal growth and dissolves other ingredients to create uniform liquid formulations.
  • 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.
  • 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 WZB9127XOA
    A synthetic red dye used to color medications and make them easier to identify. It serves as a colorant in tablets, capsules, and liquid formulations.
  • UNII H77VEI93A8
    A synthetic yellow dye used to color medications. It helps identify the drug and make it visually distinctive, with no effect on how the medicine works.
  • UNII 4F6FC4MI8W
    Lauramine oxide is a surfactant, a substance that helps mix oil and water together. It's used in medicines to improve how ingredients blend and to help the product dissolve or spread properly.
  • 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 F8U72V8ZXP
    Potassium cocoate is a salt derived from coconut oil. It acts as a surfactant and emulsifier in medicines, helping to mix oil and water-based ingredients together and improve the product's texture and stability.
  • UNII 5965N8W85T
    Propanediol is a clear liquid organic compound derived from vegetable sources or synthesized chemically. It acts as a humectant to retain moisture, a solvent to dissolve active ingredients, and a preservative booster in liquid medications and supplements.
  • UNII 96F264O9SV
    Propyl alcohol is a clear liquid solvent derived from petroleum or grain. It helps dissolve active ingredients and other components so they mix evenly throughout the medicine.
  • UNII 55X04QC32I
    A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
  • UNII DIG6BWZ9XT
    Sodium hydroxymethylglycinate is a preservative that prevents bacterial and fungal growth in liquid medicines and personal care products. It works by releasing formaldehyde in small amounts to keep the product stable and safe during storage.
  • 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 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.

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

The official label also statesWater, Sodium Laureth Sulfate, Potassium Cocoate, Cocamidopropyl Betaine, Propanediol, Lauramine Oxide, Ethanol, Benzyl Alcohol, N-Propanol, Phenoxyethanol, Fragrance, Tetrasodium EDTA, Sodium Hydroxymethylglycinate, Monoethanolamine, Citric Acid, Sodium Hydroxide, Red #40, and Yellow #6.

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 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: 414 ml 1000 ml 1250 ml 3785 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
MICRELL Antibacterial Foam Handwash .005 mg/mL 21749-0095-22 GOJO 200 ml — — Discontinued —
GOJO Antimicrobial Foam Handwash with PCMX .005 mg/mL 21749-0521-53 GOJO 535 ml — — Discontinued —
PROVON Foaming Antimicrobial Handwash with PCMX .005 mg/mL 21749-0541-20 GOJO 2000 ml — — Discontinued —
Ecolab Keystone 5 mg/mL 47593-0465-25 Ecolab 800 ml — — FDA listed —
Ecolab 5.2 mg/mL 47593-0501-11 Ecolab 3780 ml — — FDA listed —
Ecolab Inc. 5 mg/mL 47593-0503-41 Ecolab 750 ml — — Discontinued —
Ecolab Clean Force 5 mg/mL 47593-0515-25 Ecolab 800 ml — — FDA listed —
Members Mark 5 mg/mL 47593-0573-11 Ecolab 3780 ml — — FDA listed —
Kay Foaming Antibacterial Handsoap PLUS 5 mg/mL 47593-0659-70 Ecolab 1200 ml — — FDA listed —
McD Foaming Antibacterial Handsoap 5 mg/mL 47593-0669-59 Ecolab 1250 ml — — FDA listed —
Kay QSR Antibacterial Handsoap 5 mg/mL 47593-0671-11 Ecolab 3800 ml — — FDA listed —
Qsr Foaming Antibacterial Handsoap 5 mg/mL 47593-0672-41 Ecolab 750 ml — — FDA listed —
Ecolab Foaming Antibacterial Handsoap 5 mg/mL 47593-0678-59 Ecolab 1250 ml — — FDA listed —
Rushing Foaming Antibacterial Handsoap 5 mg/mL 47593-0682-59 Ecolab 1250 ml — — FDA listed —
Kay RTU Foaming AB HandSoap 5 mg/mL 47593-0693-70 Ecolab 1200 ml — — FDA listed —
Fortress Foaming Antibacterial HandSoap 5 mg/mL 47593-0694-41 Ecolab 750 ml — — FDA listed —
CleanGenic Antibacterial Foam Hand 5 mg/.001L 60933-0050-00 Fuller 1 l — — FDA listed —
Simple Hygiene Antibacterial Foam Hand 5 mg/mL 60933-0106-01 Fuller 3790 ml — — FDA listed —
Sierra Soft Antibacterial Wash 5 g/L 70415-0001-01 CWGC 1 l — — FDA listed —
Sierrasoft Clear Antibacterial Wash Foam .5 g/100mL 70415-0901-01 CWGC 1000 ml — — FDA listed —
Hillyard Citrus Fresh Antimicrobial Foaming .5 g/100mLthis 76402-0408-12 Hillyard 2000 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

🏛️
2015
On the market since
Sep 2015
📍
2026
Currently FDA-listed
11 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
76402-0408-02 1000 mL in 1 BOTTLE, PLASTIC (76402-408-02) 2015-09-01 Active
76402-0408-03 1250 mL in 1 BOTTLE, PLASTIC (76402-408-03) 2015-09-01 Active
76402-0408-06 3785 mL in 1 JUG (76402-408-06) 2015-09-01 Active
76402-0408-12 You're viewing this 2000 mL in 1 BOTTLE, PLASTIC (76402-408-12) 2015-09-01 Active
76402-0408-82 414 mL in 1 BOTTLE, PLASTIC (76402-408-82) 2015-09-01 Active

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

Pack size FAQ

What quantity is in NDC 76402-0408-12?
NDC 76402-0408-12 contains 2000 mL — 2000 ml in 1 bottle, plastic.
What is the difference between NDC 76402-0408-12 and NDC 76402-0408-82?
Both are Hillyard Citrus Fresh Antimicrobial Foaming Chloroxylenol .5 g/100mL Liquid — the drug itself is identical. NDC 76402-0408-12 is the 2000 mL package, while NDC 76402-0408-82 is the 414 ml package.
What NDC number is used to bill for this package of Hillyard Citrus Fresh Antimicrobial Foaming Chloroxylenol .5 g/100mL Liquid?
Bill NDC 76402-0408-12 — the 11-digit billing format is 76402040812. 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 ✓ 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 FDA registers it as 76402-408-12, 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: 76402-0408-12, written without dashes as 76402040812. 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 76402-0408-12, the first segment (76402) is the labeler code FDA assigned to Hillyard GMP; the middle segment (0408) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (12) 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 Hillyard GMP. 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 414 ml (76402-0408-82), 1000 ml (76402-0408-02), 1250 ml (76402-0408-03). 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?
Hillyard GMP 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 18 words ▾

Uses • Helps reduce bacteria that potentially can cause disease • Helps prevent cross contamination by hand contact

⏱️ Dosage and Administration 57 words ▾

Directions • Apply cleaner to palm of hand. • Lather and scrub hands (including fingers, wrist, and cuticles) vigorously for 60 seconds. • Rinse with water until all cleaner is removed from hands. • Dry completely (incomplete drying may lead to chapped skin). • Children under 6 years of age should be supervised when using this product.

⚠️ Warnings 18 words ▾

Warnings • For External Use Only • Do not contaminate water, food or feed by storage and disposal.

🧪 Active Ingredient 5 words ▾

Active ingredient Chloroxylenol (.50% w/w)

🧪 Inactive Ingredients 33 words ▾

Inactive Ingredients Water, Sodium Laureth Sulfate, Potassium Cocoate, Cocamidopropyl Betaine, Propanediol, Lauramine Oxide, Ethanol, Benzyl Alcohol, N-Propanol, Phenoxyethanol, Fragrance, Tetrasodium EDTA, Sodium Hydroxymethylglycinate, Monoethanolamine, Citric Acid, Sodium Hydroxide, Red #40, and Yellow #6.

🎯 Purpose 4 words ▾

Purpose Anti-Microbial Hand Cleanser

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 76402-0403-02 · Hillyard 76402-0410-02 · Hillyard →
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.