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Great Value ULTRA DISH Liquid Antibacterial HANDSOAP crisp apple Chloroxylenol .3 g/100mL Liquid, 2218 mL — NDC 79903-0136-75 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Great Value ULTRA DISH Liquid Antibacterial HANDSOAP crisp apple Chloroxylenol .3 g/100mL Liquid, 2218 mL — NDC 79903-136-75 (Billing 79903-0136-75)

by WALMART INC. · 2218 mL in 1 BOTTLE, PLASTIC

This is a package of 2,218 mL of Great Value ULTRA DISH Liquid Antibacterial HANDSOAP crisp apple Chloroxylenol .3 g/100mL Liquid from WALMART INC., marketed since Jul 2022 and currently FDA-listed, this package's marketing is listed to end Feb 2028.

NDC 79903-0136-75
🏷️ FDA NDC (as labeled) 79903-136-75 billing pads the product segment with a zero
This package
Contains2218 mL Pack sizes4 compare ↓
Product page 79903-0136-28 Also comes in: 828 ml 79903-136-28 1180 ml 79903-136-40 2070 ml 79903-136-70
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Oct 8, 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 79903-136-75 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
79903 labeler · 136 product · 75 package
Package marketed since
Jul 21, 2022
Package marketing ended
Feb 5, 2028
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 7990313675 9
FDA record last changed
Oct 8, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 79903-136-75
Product NDC 79903-136
11-digit billing NDC 79903013675
Application # 505G(a)(3)
SPL Set ID c092e30e-bd7a-4c31-95d5-3edc2170a185
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2022-07-21
Route TOPICAL
Dosage form LIQUID
Substance CHLOROXYLENOL
Why two NDCs? The FDA registers this code as 79903-136-75 — 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 → 79903-0136-75. 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.

Clinical

🧪 What is this product?

Great Value ULTRA DISH Liquid Antibacterial Handsoap is a topical liquid soap product containing chloroxylenol, an antimicrobial ingredient. Chloroxylenol is commonly used in over-the-counter antibacterial soaps and cleansing products to reduce bacteria on the skin during handwashing. This product is marketed as an OTC monograph drug, meaning it follows FDA's established rules for antibacterial handsoap ingredients rather than being individually reviewed as a new drug 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: 828 ml 1180 ml 2070 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
79903-0136-28 79903-136-28 Main listing 828 mL in 1 BOTTLE, PLASTIC 2022-07-21 — Active
79903-0136-40 79903-136-40 1180 mL in 1 BOTTLE, PLASTIC 2022-07-21 Apr 7, 2028 Active
79903-0136-75 You're viewing this 2218 mL in 1 BOTTLE, PLASTIC 2022-07-21 Feb 5, 2028 Active
79903-0136-70 79903-136-70 2070 mL in 1 BOTTLE, PLASTIC 2026-01-29 — Active

You're viewing the largest of 4 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 2218 mL — 2218 ml in 1 bottle, plastic.
How does this package differ from NDC 79903-0136-28?
Both are Great Value ULTRA DISH Liquid Antibacterial HANDSOAP crisp apple Chloroxylenol .3 g/100mL Liquid — the drug itself is identical. This page's package is the 2218 mL one, while NDC 79903-0136-28 is the 828 ml package.
What NDC number is used to bill for this package of Great Value ULTRA DISH Liquid Antibacterial HANDSOAP crisp apple Chloroxylenol .3 g/100mL 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
Triclosan Free Antibacterial 7.5 oz (Fresh Citrus) Antibacterial .3 g/100mL 57337-0090-01 Rejoice 221 ml — — FDA listed —
Great Value ULTRA DISH Liquid Antibacterial HANDSOAP crisp apple .3 g/100mLthis 79903-0136-75 WALMART 2218 ml — — FDA listed —
Triclosan Free Antibacterial Antibacterial .3 g/100mL 57337-0086-01 Rejoice 443 ml — — FDA listed —
Zep Applaud AB .3 g/100mL 66949-0123-01 Zep 11400 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 original Antibacterial .3 g/100mL 57337-0087-01 Rejoice 221 ml — — FDA listed —
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 —
Triclosan Free Antibacterial 7.5 oz (Strawberry Pomegranate) Antibacterial .3 g/100mL 57337-0089-01 Rejoice 221 ml — — 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 —
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

🏛️
2022
On the market since
Jul 2022
📍
2026
Currently FDA-listed
4 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.

What it looks like

Color green
FlavorApple
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

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 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 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 60NSK897G9
    A synthetic detergent-like chemical that acts as a surfactant and solubilizer in medicines. It helps dissolve or suspend active ingredients and improve how the drug spreads through the formulation.
  • 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 H3R47K3TBD
    FD&C Blue No. 1 is a synthetic blue dye approved for use in foods and medicines. It serves as a colorant to give the medication its distinctive appearance and help with product identification.
  • UNII I753WB2F1M
    FD&C Yellow No. 5 is a synthetic yellow colorant approved by the FDA. It is added to medicines to make pills, tablets, or liquids visually distinct and easier to identify.
  • 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.
  • 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 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 ZZQ59TY3KG
    Sodium laureth-2 sulfate is a cleansing agent made from coconut oil. It helps medicines dissolve properly and can reduce foaming or improve how the product spreads on skin.
  • UNII 368GB5141J
    A detergent and foaming agent derived from coconut or palm oil. In medications, it helps break down and mix oil and water-based ingredients, aids in tablet disintegration, and improves how the drug dissolves and spreads in the mouth or digestive system.
  • UNII G4LZF950UR
    Sodium xylenesulfonate is a synthetic organic salt used as a solubilizer and buffering agent in liquid medications. It helps dissolve active ingredients that don't mix well with water, improving how the medicine can be formulated and absorbed.
  • 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.

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

The official label also statesWATER, SODIUM C10-16 ALKYLBENZENE SULFONATE, SODIUM LAURETH SULFATE, COCAMIDOPROPYL BETAINE, SODIUM LAURYL SULFATE, SODIUM XYLENESULFONATE, PROPYLENE GLYCOL, SODIUM CHLORIDE, FRAGRANCE, CITRIC ACID, TETRASODIUM EDTA, METHYLISOTHIAZOLINONE/METHYLCHLOROISOTHIAZOLINONE, YELLOW 5, BLUE 1.

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

LabelerWALMART INC.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code79903
First marketedJul 2022
Product typeHuman Otc Drug
Portfolio192 products on file

More NDCs from WALMART INC. labeler code 79903

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 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 9 words ▾

Uses for handwashing to decrease bacteria on the skin

⏱️ Dosage and Administration 15 words ▾

Directions • wet hands • apply palmful to hands • scrub thoroughly • rinse thoroughly

⚠️ Warnings 65 words ▾

Warnings For external use only: hands only When using this product • do not get into eyes. If contact occurs, rinse eyes thoroughly 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 4 words ▾

Active ingredient Chloroxylenol 0.3%

🧪 Inactive Ingredients 31 words ▾

Inactive ingredients WATER, SODIUM C10-16 ALKYLBENZENE SULFONATE, SODIUM LAURETH SULFATE, COCAMIDOPROPYL BETAINE, SODIUM LAURYL SULFATE, SODIUM XYLENESULFONATE, PROPYLENE GLYCOL, SODIUM CHLORIDE, FRAGRANCE, CITRIC ACID, TETRASODIUM EDTA, METHYLISOTHIAZOLINONE/METHYLCHLOROISOTHIAZOLINONE, YELLOW 5, BLUE 1.

🎯 Purpose 2 words ▾

Purpose Antibacterial

📄 Keep Out of Reach of Children 20 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 5 words ▾

Packaging Great Value ULTRA DISH

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Chloroxylenol — the ingredient across all brands.

Top reported reactions

Vomiting7
Erythema6
Malaise6
Nausea5
Pain5
Renal Failure5
Weight Decreased5

Age at onset

Child1
Adult1
Elderly1

Reporter sex

78 reports
Male · 31%
Female · 69%

Serious outcomes

Hospitalization24
Life-threatening7
Death5
Disabling1
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 6 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

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 WALMART 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 3 other package presentations of this same product, including 828 ml (79903-0136-28), 1180 ml (79903-0136-40), 2070 ml (79903-0136-70). 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?
WALMART 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.
← 79903-0135-08 · Walmart 79903-0137-24 · WAL-MART →
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.