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Renown Antibacterial Hand CHLOROXYLENOL 3000 mg/L Liquid, 3.78 l — NDC 18949-0051-00 package photo

Renown Antibacterial Hand CHLOROXYLENOL 3000 mg/L Liquid, 3.78 l

by HD Supply · 3.78 L in 1 BOTTLE (18949-051-00)
NDC 18949-0051-00
🏷️ FDA NDC (as labeled) 18949-051-00 billing pads the product segment with a zero
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) 18949-051-00
Product NDC 18949-051
11-digit billing NDC 18949005100
RxCUI 413261
UNII 0F32U78V2Q
UPC 0194671047423
Application # 505G(a)(3)
SPL Set ID 6b47593c-b1d0-4c6a-b485-4d0797544cc7
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-09-28
Route TOPICAL
Dosage form LIQUID
Substance CHLOROXYLENOL
Why two NDCs? The FDA registers this code as 18949-051-00 — 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 → 18949-0051-00. 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

LabelerHD Supply
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code18949
First marketedSep 2023
Product typeHuman Otc Drug
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?

Renown Antibacterial Hand is a topical liquid containing chloroxylenol, an antimicrobial agent typically used in hand soaps and sanitizing products. This is an over-the-counter monograph drug, meaning it is marketed under FDA's established guidelines for antiseptic hand-cleaning products rather than as an individually approved application. Chloroxylenol is commonly included in antibacterial formulations intended for routine hand washing and sanitizing.

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 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 21X4Y0VTB1
    A surfactant derived from coconut oil that helps mix oil and water components. It's used in formulations as an emulsifier and foam booster to improve product texture and stability.
  • UNII 9DBA0SBB0L
    A synthetic red dye derived from coal tar used as a colorant in medicines and cosmetics. It gives tablets, capsules, and liquids their red or pink appearance for identification and visual appeal.
  • 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 77CBG3UN78
    Magnesium nitrate is a salt compound that acts as a buffer and pH regulator in medicines. It helps maintain the proper acidity level to keep the drug stable and effective in its dosage form.
  • UNII DEL7T5QRPN
    A synthetic preservative that kills bacteria and fungi. It's added to medications to prevent microbial growth and extend shelf life, especially in liquid or topical formulations.
  • UNII 229D0E1QFA
    Methylisothiazolinone is a synthetic chemical preservative that prevents bacterial and fungal growth in liquid medicines and topical products. It helps keep the medication safe and extends shelf life during storage.
  • UNII 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
  • 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 0YPR65R21J
    Sodium sulfate is a mineral salt used in pharmaceuticals as a filler and diluent. It helps provide bulk and stability to tablets and capsules while remaining inert in the body.
  • 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 statesDEIONIZED WATER, SODIUM LAURYL ETHER SULFATE, SODIUM CHLORIDE, COCAMIDE MIPA, SODIUM SULFATE, OCEAN BREEZE FRAGRANCE 16295, MAGNESIUM NITRATE, CITRIC ACID, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, FD & C YELLOW #6, D&C RED NO. 33

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.
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
Lemon Drop Gentle Antiseptic 3 mg/mL 11429-1006-01 Woodbine 118 ml — — FDA listed —
Simplify Antibacterial Hand Apple Blossom Scent .3 g/100mL 11822-0281-01 Rite 573 ml — — Discontinued —
Antiseptic Hand 3 mg/mL 16496-0544-14 Image 3785 ml — — FDA listed —
Renown Antibacterial Hand 3000 mg/Lthis 18949-0051-00 HD 3.78 l — — FDA listed —
Symmetry Antimicrobial Foaming Hand Wash .3 g/100mL 30805-0006-02 Buckeye 1250 ml — — FDA listed —
Altra Antimicrobial Foaming Hand Wash with 0.3% PCMX .3 g/100mL 30805-0016-02 Buckeye 1250 ml — — Discontinued —
Sentry Antiseptic Handsoap 3 mg/mL 31507-0544-14 Wechem, 3785 ml — — FDA listed —
Hand Guard High Foaming Antiseptic Hand and Body Wash 3 mg/mL 31507-0876-01 Wechem, 1200 ml — — Discontinued —
Chloroxylenol 0.30 % 3 mg/mL 42669-0028-03 Davion, 828 ml — — FDA listed —
Fm-24 Foaming 3 mg/mL 43097-0876-01 People's 1200 ml — — Discontinued —
Sani Foam Mango Antiseptic Hand and Body Wash 3 mg/mL 43374-0876-10 Delta 1000 ml — — Discontinued —
Pearl Antimicrobial Hand Item 1027Ab-01 .3 g/100mL 50536-0127-01 AMERICAN 3785 ml — — FDA listed —
Soft Touch Plus Antibacterial Hand Item 1039 .3 g/100mL 50536-0139-01 AMERICAN 3785 ml — — FDA listed —
Super Suds Antibacterial Hand Item 1063 .3 g/100mL 50536-0163-01 AMERICAN 3785 ml — — FDA listed —
E-2 Hand Item 1095 .3 g/100mL 50536-0195-01 AMERICAN 3785 ml — — FDA listed —
Golden Medicated .3 g/100mL 50865-0060-09 Kutol 3785 ml — — FDA listed —
Xtra Antibacterial Hand Juicy Orange 3 mg/mL 51628-0033-00 MY 709 ml — — FDA listed —
Ultra 3 mg/mL 55910-0589-44 Old 532 ml — — FDA listed —
Triclosan Free Antibacterial Antibacterial .3 g/100mL 57337-0086-01 Rejoice 443 ml — — FDA listed —
Triclosan Free Antibacterial 7.5 oz original Antibacterial .3 g/100mL 57337-0087-01 Rejoice 221 ml — — FDA listed —
Triclosan Free Antibacterial 7.5 oz (Ocean) Antibacterial .3 g/100mL 57337-0088-01 Rejoice 221 ml — — FDA listed —
Triclosan Free Antibacterial 7.5 oz (Strawberry Pomegranate) Antibacterial .3 g/100mL 57337-0089-01 Rejoice 221 ml — — FDA listed —
Triclosan Free Antibacterial 7.5 oz (Fresh Citrus) Antibacterial .3 g/100mL 57337-0090-01 Rejoice 221 ml — — FDA listed —
Chemseptic 3 mg/mL 59503-0544-01 Rochester 532 ml — — Discontinued —
Antibacterial Foamy Mango High Foaming Antiseptic Hand and Body Wash 3 mg/mL 60456-0876-01 Carpet 1200 ml — — Discontinued —
Franklin cleaning technology antibacterial hand 3 mg/mL 60933-0056-00 Fuller 3790 ml — — FDA listed —
1012 Antimicrobial 3 mg/mL 62257-0012-06 ABC 800 ml — — Discontinued —
Lynx Antibacterial 3 mg/mL 62257-0160-01 ABC 1200 ml — — Discontinued —
Lynx Foamy PCMX Antiseptic Hand and Body Wash 6876 3 mg/mL 62257-0161-01 ABC 1200 ml — — Discontinued —
LX0380 Lynx glacier fresh Antiseptic Hand and Body Wash 6380 3 mg/mL 62257-0380-12 ABC 1000 ml — — FDA listed —
Palm 3 mg/mL 62257-0544-06 ABC 800 ml — — FDA listed —
Lynx LX0864 peachy-foam antiseptic handsoap 3 mg/mL 62257-0686-12 ABC 1000 ml — — FDA listed —
Sani Mango Antiseptic Hand and Body Wash 3 mg/mL 62257-0875-01 ABC 1200 ml — — Discontinued —
Sani Mango Antiseptic Hand and Body Wash 3 mg/mL 62257-0876-01 ABC 1200 ml — — FDA listed —
Handtastic Foamy Mango Antiseptic Hand and Body Wash 3 mg/mL 63533-0876-01 Momar 1200 ml — — Discontinued —
Suds High Foaming Antiseptic Hand and Body Wash 3 mg/mL 63830-0876-01 Pro 1200 ml — — Discontinued —
Fresh Start 3 mg/mL 63830-0950-06 Pro 800 ml — — FDA listed —
Surgent Antiseptic 3 mg/mL 66155-0544-01 SunCoast 1200 ml — — Discontinued —
Zep Applaud AB .3 g/100mL 66949-0123-01 Zep 11400 ml — — FDA listed —
Inoderm Style Antibacterial 3 mg/.001L 73062-0055-00 Avro 3.8 l — — FDA listed —
Inoderm Choice Antibacterial 3 mg/mL 73062-0523-42 Avro 3800 ml — — FDA listed —
Kroger Antibacterial Green Apple Hand .3 g/100mL 73487-0001-01 Korex 709 ml — — Discontinued —
Power Force Antibacterial Handsoap Green Apple Scent .3 g/100mL 73487-0008-01 Korex 709 ml — — FDA listed —
Power Force Antibacterial Handsoap Citrus Scent .3 g/100mL 73487-0009-01 KOREX 709 ml — — FDA listed —
Freshands Premium Foamy Antibacterial Handsoap 6876 3 mg/mL 75632-0876-14 Consolidated 3785 ml — — Discontinued —
Satin Foam High Foaming Antiseptic Hand Wash 3 mg/mL 75990-0914-03 Certus 750 ml — — FDA listed —
Green Antibacterial Dish and HandSoap 30 mg/10mL 79481-0200-02 Meijer, 709 ml — — FDA listed —
TOTO Antibacterial Foam HandSoap 3 mg/mL 84791-0686-05 Toto 18927 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

🏛️
2023
On the market since
Sep 2023
📍
2026
Currently FDA-listed
3 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
18949-0051-00 You're viewing this 3.78 L in 1 BOTTLE (18949-051-00) 2023-09-28 Active

🧭 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 18949-051-00, 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: 18949-0051-00, written without dashes as 18949005100. 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 18949-0051-00, the first segment (18949) is the labeler code FDA assigned to HD Supply; the middle segment (0051) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (00) 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 HD Supply. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
HD Supply 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 14 words ▾

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

⏱️ Dosage and Administration 30 words ▾

DIRECTIONS Pump a small amount of foam into palm of hand Rub thoroughly over all surfaces of both hands Rub hands together to produce a thick lather Rinse and repeat

⚠️ Warnings 56 words ▾

Warnings For external use only Do not use in the eyes. In case of contact, flush eyes with water. Stop use and ask a doctor if irritation and redness develop condition persists for more than 72 hours KEEP OUT OF REACH OF CHILDREN If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 6 words ▾

Active ingredient Chloroxylenol 0.3% Purpose Antiseptic

🧪 Inactive Ingredients 33 words ▾

Inactive ingredients DEIONIZED WATER, SODIUM LAURYL ETHER SULFATE, SODIUM CHLORIDE, COCAMIDE MIPA, SODIUM SULFATE, OCEAN BREEZE FRAGRANCE 16295, MAGNESIUM NITRATE, CITRIC ACID, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, FD & C YELLOW #6, D&C RED NO. 33

🎯 Purpose 2 words ▾

Purpose Antiseptic

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 18657-0117-04 · Antares 19188-0123-01 · All →
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.