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KleenLine Essentials Foaming Hand Sanitizer Ethyl Alcohol .7 mL/mL Liquid, 1000 mL — NDC 79258-0802-29 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

KleenLine Essentials Foaming Hand Sanitizer Ethyl Alcohol .7 mL/mL Liquid, 1000 mL — NDC 79258-802-29 (Billing 79258-0802-29)

by Brady Industries · 1000 mL in 1 BAG

This is a package of 1,000 mL of KleenLine Essentials Foaming Hand Sanitizer Ethyl Alcohol .7 mL/mL Liquid from Brady Industries, marketed since Dec 2024 and currently FDA-listed. It is this product's only package size.

NDC 79258-0802-29
🏷️ FDA NDC (as labeled) 79258-802-29 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 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 79258-802-29 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
79258 labeler · 802 product · 29 package
Package marketed since
Dec 16, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0810037737004, 0651619016021
FDA record last changed
Jul 24, 2026
⚠️
Other active recalls for Ethyl Alcohol (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · May 23, 2025 — Subpotent product: Product has cloudy appearance and tested below assay label claim for 70% Ethyl Alcohol (Consumer Product Partners, LLC) · FDA recall D-0458-2025
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 79258-802-29
Product NDC 79258-802
11-digit billing NDC 79258080229
RxCUI 616805
UNII 3K9958V90M
UPC 0810037737004, 0651619016021
Application # 505G(a)(3)
SPL Set ID 2969ce5b-39b4-47b7-e063-6394a90a1909
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-12-16
Route TOPICAL
Dosage form LIQUID
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 616805
Why two NDCs? The FDA registers this code as 79258-802-29 — 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 → 79258-0802-29. 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

📗 Our plain-language guide HelloPharmacist
  • It depends on the product. Hand sanitizers and wipes help reduce bacteria on your skin, and alcohol pads prepare skin before an injection. A separate injected form is used by heart...
  • Most directions say to cover all surfaces of your hands and rub until dry. Sprays and wipes follow similar steps. Check your product's label, since directions differ a bit between...
  • Children under 6 should use hand sanitizer only with adult supervision to avoid swallowing. Keep all products out of reach of children. If someone swallows it, get medical help or...
  • Stop using it and ask a doctor if you get irritation and redness, or if your condition lasts more than 72 hours. Avoid broken skin and keep it out of your eyes. If it gets in your...
📖 Read our full Alcohol guide →

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.
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
79258-0802-29 You're viewing this Main listing 1000 mL in 1 BAG 2024-12-16 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
PURELL Advanced E3 Rated Instant Hand Sanitizer Foam .7 mL/mL 21749-0802-51 GOJO 550 ml — — Discontinued —
PURELL Advanced Green Certified Instant Hand Sanitizer .7 mL/mL 21749-0806-51 GOJO 550 ml — — Discontinued —
PURELL Advanced Instant Hand Sanitizer .7 mL/mL 21749-0807-17 GOJO 515 ml — — FDA listed —
PURELL Healthcare Advanced Hand Sanitizer Foam .7 mL/mL 21749-0811-45 GOJO 450 ml — — Discontinued —
PURELL Healthcare Advanced Hand Sanitizer Gentle and Free Foam .7 mL/mL 21749-0822-53 GOJO 535 ml — — FDA listed —
PURELL Advanced Hand Sanitizer Gentle and Free Foam .7 mL/mL 21749-0826-53 GOJO 535 ml — — FDA listed —
PURELL Advanced Hand Sanitizer Fragrance Free Foam .7 mL/mL 21749-0827-17 GOJO 515 ml — — FDA listed —
PURELL Advanced Hand Sanitizer Moisturizing 2in1 Foam 70 mL/100mL 21749-0851-10 GOJO 295 ml — — FDA listed —
PURELL Healthcare Advanced Hand Sanitizer ULTRA NOURISHING Foam .7 mL/mL 21749-0854-53 GOJO 535 ml — — FDA listed —
PURELL Advanced Hand Sanitizer ULTRA NOURISHING Foam 70 mL/100mL 21749-0856-17 GOJO 515 ml — — FDA listed —
PURELL Advanced Hand Sanitizer Naturals Foam 70 mL/100mL 21749-0875-10 GOJO 295 ml — — FDA listed —
Symmetry Foaming Hand Sanitizer Fragrance Free 70 mL/100mL 30805-0020-04 Buckeye 1200 ml — — FDA listed —
Symmetry Foaming Hand Sanitizer 70 mL/100mL 30805-0021-09 Buckeye 1000 ml — — FDA listed —
Altra Foaming Hand Sanitizer Fragrance Free with Aloe and Vitamin E 70 mL/100mL 30805-0023-07 Buckeye 550 ml — — FDA listed —
I-70 Foaming .7 mL/mL 43097-0968-12 People's 1000 ml — — FDA listed —
ESC Protecting Foam Hand Sanitizer 76.9 mL/100mL 47593-0667-41 Ecolab 750 ml — — FDA listed —
Ecolab Retail Foaming Alcohol Hand Sanitizer 70 mL/100mL 47593-0685-56 Ecolab 1200 ml — — FDA listed —
Kay Alcohol Foam Hand Sanitizer 70 mL/100mL 47593-0686-56 Ecolab 1200 ml — — FDA listed —
Tork Hand Sanitizing Alcohol Foam 70 mL/100mL 49351-0301-01 Essity 1000 ml — — FDA listed —
Foaming Hand Sanitizer 70 mL/100mL 50021-0020-01 Empack 550 ml — — FDA listed —
MG FoamSan 70 .7 L/L 50241-0223-02 Morgan 3.785 l — — FDA listed —
EnMotion Foam Hand Sanitizer 70 mL/100mL 54622-0120-01 Georgia-Pacific 1000 ml — — FDA listed —
enMotion Foam High Frequency Use .7 mL/mL 54622-0121-01 Georgia-Pacific 2 bottles — — FDA listed —
Pacific Blue Ultra Foaming Fragrance Free 70 mg/mL 54622-0122-01 Georgia-Pacific 1000 ml — — FDA listed —
Pacific Blue Select Foam Hand Sanitizer, Fragrance Free, Dye Free 70 mL/100mL 54622-0311-01 Georgia-Pacific 24 bottles — — FDA listed —
enMotion Foam High Frequency Use 70 mL/100mL 54622-0486-01 Georgia-Pacific 1000 ml — — FDA listed —
Kleenex Ultra Moisturizing Hand Sanitizer 70 mL/100mL 55118-0530-10 Kimberly-Clark 1000 ml — — Discontinued —
Kleenex Reveal Moisturizing Foam Hand Sanitizer 70 mL/100mL 55118-0531-10 Kimberly-Clark 6 bottles — — Discontinued —
Lynx san a foam .7 mL/mL 62257-0007-10 ABC 1000 ml — — FDA listed —
Fast .7 mL/mL 62257-0658-08 ABC 1000 ml — — Discontinued —
Dermacen Foaming Instant Hand Sanitizer With Aloe 70 mL/100mL 62654-0149-13 Central 1000 ml — — FDA listed —
Saniclean 70 g/100mL 63900-0150-02 Simoniz 1000 ml — — FDA listed —
Foaming Instant Hand Sanitizer with Aloe 70 g/100g 68599-5205-01 MCKESSON 251 g — — FDA listed —
Hand Sanitizer 70 mL/100mL 69790-0456-44 Uline 532 ml — — FDA listed —
EXTENDED CARE Foaming Hand Sanitizer .7 mL/mL 71875-0800-40 TRIPLE 1200 ml — — FDA listed —
Hand Sanitizer 70 mL/100mL 71897-0465-86 Veritiv 1000 ml — — FDA listed —
Clean Revolution Foaming Hand Sanitizer Refill Supply Container - Gentle and Aloe Enriched - ELIMINATES 99.9% Germs - 70% Ethanol - Ready To Use 70 mL/100mL 74810-0725-00 Replenish 3785 ml — — FDA listed —
Recens Foam .7 mL/mL 75990-0968-07 Certus 700 ml — — Discontinued —
Hand Sanitizer 70 mL/100mL 76370-0003-01 Tazza 10000 ml — — Discontinued —
Hand Sanitizer 70 mL/100mL 76370-0005-02 Tazza 3785 ml — — Discontinued —
Tazza 70% Alcohol-Based Hand Sanitizing Foam 70 L/100L 76370-0033-00 Tazza 3.785 l — — FDA listed —
Hand Sanitizer Foam 70 mL/100mL 77955-0002-02 Custom 1000 ml — — FDA listed —
Ops 70 Percent Alcohol Foaming Skin Sanitizer 70 mL/100mL 79016-0101-12 Archer 1000 ml — — FDA listed —
Black Ops 70 Percent Alcohol Foaming Skin Sanitizer 70 mL/100mL 79016-0102-12 Archer 1000 ml — — FDA listed —
KleenLine Essentials Foaming Hand Sanitizer .7 mL/mLthis 79258-0802-29 Brady 1000 ml — — FDA listed —
MyHealth Advanced Hand Sanitizer 70 mL/100mL 80661-0002-01 Aeroflex 150 ml — — FDA listed —
Novo Foaming Instant Hand Sanitizer .7 mL/mL 81551-0802-04 Noble 3785 ml — — FDA listed —
Foaming Hand Alcohol Foam 70 mL/100mL 83019-0102-11 Draco 1000 ml — — FDA listed —
AMORA Hand Sanitizer Mist Cherry .7 mL/mL 85161-0171-01 Longway 45 ml — — FDA listed —
AMORA Hand Sanitizer Mist Strawberry .7 mL/mL 85161-0168-01 Longway 45 ml — — FDA listed —
Surface Hand Sanitizer Caramel Latte .7 mL/mL 85161-0172-01 Longway 45 ml — — FDA listed —
Surface Hand Sanitizer Surprise .7 mL/mL 85161-0174-01 Longway 45 ml — — FDA listed —
AMORA Hand Sanitizer Mist Watermelon .7 mL/mL 85161-0170-01 Longway 45 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

🏛️
2024
On the market since
Dec 2024
📍
2026
Currently FDA-listed
2 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.

🧪 Avoiding an ingredient? See Alcohol inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

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

  • UNII 5WA6R1KL5J
    A synthetic organic compound used as a solvent in pharmaceutical formulations. It helps dissolve or suspend active ingredients and other components to create a uniform, stable medicine.
  • UNII HFL24LW6V5
    A synthetic organic alcohol used as a solvent and preservative in medications. It helps dissolve active ingredients and protects the medicine from microbial contamination during storage.
  • UNII RUE8E6T4NB
    Aloe vera leaf juice is a clear gel extracted from aloe vera plant leaves. It's used in medicines as a lubricant, emollient, and preservative to soothe skin contact and help keep the product stable.
  • UNII 2JDK5W22H4
    A silicone-based substance that reduces surface tension and helps distribute ingredients evenly throughout the formula. It serves as an emulsifier and anti-foaming agent in medications.
  • UNII 8J6RDU8L9X
    A synthetic green dye used to color medications. It helps make pills and capsules visually distinct so patients can easily identify their medicine.
  • UNII 28N247O58B
    A synthetic alcohol used as a solvent and preservative in liquid medicines. It helps dissolve active ingredients and prevents microbial growth in the formulation.
  • UNII 7U7KU3MWT0
    Hexyl acetate is a synthetic liquid compound used as a solvent and flavoring agent in medicines. It helps dissolve other ingredients and can contribute to the taste or aroma of the formulation.
  • UNII 8SQ0VA4YUR
    A fragrance compound derived from natural sources, used to add pleasant scent to the medicine. It serves as a flavoring or aromatic agent to mask unpleasant tastes or improve the product's sensory appeal.
  • UNII 8PR7V1SVM0
    A silicone-based lubricant combined with polyethylene glycol. It reduces friction and helps the medicine flow smoothly during manufacturing and improves how the product feels when applied or swallowed.
  • 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 UM4XS5M134
    A synthetic fragrance ingredient derived from linalool, a naturally occurring compound found in plants. It functions as a fragrance component and masking agent to improve the smell and taste appeal of the medicine.
  • UNII 2NDV3959AX
    A synthetic fragrance compound used to add scent to medicines. It functions as a flavoring or masking agent to make the medication more pleasant to taste or smell.
  • 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, PEG-10 Acrylate/Perfluorohexylethyl/acrylate polymer, Perfluorohexyl Alcohol, Propylene Glycol, Fragrance, Aloe Barbadensis Leaf Juice, D&C Green 5,

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

LabelerBrady Industries
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code79258
First marketedDec 2024
Product typeHuman Otc Drug
Portfolio5 products on file

More NDCs from Brady Industries labeler code 79258

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 📖 Instructions for Use 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 18 words ▾

usage Hand sanitizer to reduce microorganisms on skin Use this product when soap and water are not available

⏱️ Dosage and Administration 16 words ▾

Place enough product on your palms to thoroughly cover hands rub hands together briskly until dry

⚠️ Warnings 16 words ▾

For external use only. FLAMMABLE. This product contains ethyl alcohol. Keep away from heat or flame

🧪 Active Ingredient 2 words ▾

Ethyl Alcohol

🧪 Inactive Ingredients 16 words ▾

Water, PEG-10 Acrylate/Perfluorohexylethyl/acrylate polymer, Perfluorohexyl Alcohol, Propylene Glycol, Fragrance, Aloe Barbadensis Leaf Juice, D&C Green 5,

🎯 Purpose 1 words ▾

Antiseptic

📄 Keep Out of Reach of Children 18 words ▾

Keep out of reach of children if swalllowed cget medical help or contact Poison Control Center righ away

📖 Instructions for Use 24 words ▾

Read entire label before using this product Place enough product on your palm to thoroughly cover your hands Rub hands together briskly until dry

📄 Package Label / Principal Display Panel 2 words ▾

label label

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 Brady Industries. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Brady Industries 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.
← 79258-0709-29 · Brady 79258-0817-04 · Brady →
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.