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PURELL Cottony Soft Hand Sanitizing Wipe alcohol 62 mL/100mL Cloth — NDC 21749-0364-76 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

PURELL Cottony Soft Hand Sanitizing Wipe alcohol 62 mL/100mL Cloth — NDC 21749-364-76 (Billing 21749-0364-76)

by GOJO Industries, Inc. · 1 POUCH in 1 PACKAGE / 4 mL in 1 POUCH

This is a package of PURELL Cottony Soft Hand Sanitizing Wipe alcohol 62 mL/100mL Cloth from GOJO Industries, Inc., marketed since Feb 2012 and currently FDA-listed. It is this product's only package size.

NDC 21749-0364-76
🏷️ FDA NDC (as labeled) 21749-364-76 billing pads the product 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) 21749-364-76
Product NDC 21749-364
11-digit billing NDC 21749036476
RxCUI 1041780
UNII 3K9958V90M
Application # 505G(a)(3)
SPL Set ID fc19689f-4826-4adf-8292-ea002cc4ad05
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2012-02-24
Route TOPICAL
Dosage form CLOTH
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 1041780
Why two NDCs? The FDA registers this code as 21749-364-76 — 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 → 21749-0364-76. 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 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
21749-0364-76 You're viewing this Main listing 1 POUCH in 1 PACKAGE / 4 mL in 1 POUCH 2012-02-24 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
PURELL Hand Sanitizing Wipe 62 mL/100mL 21749-0363-76 GOJO 1 pouch — — FDA listed —
PURELL Cottony Soft Hand Sanitizing Wipe 62 mL/100mLthis 21749-0364-76 GOJO 1 pouch — — FDA listed —
PURELL Hand Sanitizing Wipes Alcohol Formula 62 mL/100mL 21749-0367-36 GOJO 101 ml — — FDA listed —
Medline 62 mL/100mL 53329-0121-09 Medline 1 applicator — — FDA listed —
EO Hand Sanitizer Wipes Lavender 62 mL/100mL 54748-0502-01 EO 3 ml — — FDA listed —
everyone hand sanitizer wipes coconut lemon 62 mL/100mL 54748-0701-15 EO 6 packets — — FDA listed —
everyone hand sanitizer wipes lavender aloe 62 mL/100mL 54748-0702-15 EO 6 packets — — FDA listed —
everyone hand sanitizer wipes ruby grapefruit 62 mL/100mL 54748-0703-15 EO 6 packets — — FDA listed —
CareTouch .62 mL/mL 60913-0026-11 Phoenix 110 packets — — FDA listed —
Hand Sanitizing Wipes .62 mL/mL 60913-0415-11 PHOENIX 110 packets — — FDA listed —
Hand Sanitizing Wipes .62 mL/mL 60913-0416-11 Phoenix 100 packets — — FDA listed —
CareTouch .62 mL/mL 70393-0415-11 Future 110 packets — — FDA listed —
Nozin Nasal Sanitizer (Antiseptic) 62 mL/100mL 82539-0211-02 Global 250 ampules — — FDA listed —
SaniiSwab .62 g/g 84456-0746-02 POLLEY 100 packets — — FDA listed —
SaniiSwab .62 g/g 87051-0001-50 PolleyMed 50 packets — — FDA listed —
SaniiSwab .62 g/g 87051-0002-10 PolleyMed 10 packets — — FDA listed —
QUR Lavender essential oil hand sanitizer 62 mL/100mL 81761-0111-01 Qur, 30 ml — — FDA listed —
QUR Vanilla essential oil hand sanitizer 62 mL/100mL 81761-0112-01 Qur, 30 ml — — FDA listed —
Strawberry Pound Cake SCENTED HAND SANITIZER 62 mL/100mL 85588-0203-01 MELON 29 ml — — FDA listed —
Hand Sanitizer 62 mL/100mL 77955-0001-02 Custom 1000 ml — — FDA listed —
Hand Sanitizer 62 mL/100mL 83986-0652-04 UpLift 750 ml — — FDA listed —
Hand Sanitizer Lemon Scented 62 mL/100mL 87614-0002-01 Taizhou 60 ml — — FDA listed —
Instant Hand Antiseptic 62 mL/100mL 59448-0001-02 ASP 53 ml — — FDA listed —
Instant Hand Antiseptic 62 mL/100mL 59448-0004-01 ASP 53 ml — — FDA listed —
antibacterial hand sanitizer gel 01 62 mL/100mL 82953-0022-01 Cosmuses 15 ml — — FDA listed —
Vanilla Sugar SCENTED HAND SANITIZER 62 mL/100mL 85588-0202-01 MELON 29 ml — — FDA listed —
Sanitaxe 27 Oz Instant Hand Sanitizer With Aloe Vera 62 mL/100mL 72197-0032-27 American 800 ml — — FDA listed —
Pink Pineapple SCENTED HAND SANITIZER 62 mL/100mL 85588-0201-01 MELON 29 ml — — FDA listed —
Genuine First Aid Hand Sanitizer 62 mL/100mL 50814-0078-01 GFA 1.03 ml — — FDA listed —
EO HAND SANITIZER Unscented 62 mL/100mL 54748-0203-07 EO 946 ml — — FDA listed —
Hand Sanitizer 62 mL/100mL 73288-0008-01 NINGBO 500 packets — — FDA listed —
Servo-Stat 62 mL/100mL 76378-0015-01 Enzyme 118 ml — — FDA listed —
Hand Sanitizer with Aloe 62 mL/100mL 83986-0826-16 UpLift 59 ml — — FDA listed —
EOCENE Dr. HANITIZER 62 mL/100mL 73466-0006-01 MISOCOS 100 ml — — FDA listed —
health beyond HAND SANITIZER 62 mL/100mL 43473-0075-01 Nantong 500 packets — — FDA listed —
Sanifoam Hand Sanitizer 62 mL/100mL 50536-0078-01 AMERICAN 3785 ml — — FDA listed —
Hand Sanitizer Rebel Cherry 62 mL/100mL 76891-0136-11 SCENT 29 ml — — FDA listed —
antibacterial hand sanitizer gel 01 62 mL/100mL 82953-0016-01 Cosmuses 15 ml — — FDA listed —
Hand Sanitizer Coconut Breeze 62 mL/100mL 76891-0135-11 SCENT 29 ml — — FDA listed —
Mada 62 mL/100mL 11928-0004-04 Mada 118 ml — — FDA listed —
Aosi Healthcare Hand Sanitizer 62 mL/100mL 43473-0056-01 Nantong 9 ml — — FDA listed —
EO HAND SANITIZER Lavender 62 mL/100mL 54748-0201-05 EO 59 ml — — FDA listed —
Hand Sanitizing with Lavender Oil 62 mL/100mL 59088-0413-06 PureTek 1 bottle — — FDA listed —
Pharmacys Prescription 8Oz Hand Sanitizer 62 mL/100mL 72197-0011-08 American 237 ml — — FDA listed —
Sweet Coconut SCENTED HAND SANITIZER 62 mL/100mL 85588-0204-01 MELON 29 ml — — FDA listed —
Prevent Hand Sanitizer 62 mL/100mL 50536-0077-12 AMERICAN 3785 ml — — FDA listed —
Instant Hand Antiseptic 62 mL/100mL 59448-0008-01 ASP 53 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

🏛️
2012
On the market since
Feb 2012
📍
2026
Currently FDA-listed
14 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.

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

  • UNII A7E6112E4N
    A form of vitamin E used as an antioxidant in medicines. It prevents oils and fats in the product from breaking down, helping maintain stability and shelf life.
  • UNII A9EJ3J61HQ
    A synthetic liquid derived from benzoic acid and long-chain alcohols. It functions as a solvent and penetration enhancer in topical formulations, helping active ingredients dissolve and absorb into the skin.
  • UNII ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • UNII LU49E6626Q
    A synthetic organic compound used as a pH buffer and neutralizing agent in medicines. It helps maintain the proper acidity level in liquid formulations to improve stability and comfort.
  • UNII X7GNG3S47T
    A quaternary ammonium compound used as an antistatic agent and emulsifier in pharmaceutical formulations. It helps reduce static electricity during manufacturing and improves texture or consistency in creams and lotions.
  • UNII H2KVQ74JM4
    A compound derived from coconut oil that acts as a conditioning agent and surfactant. It helps stabilize and thicken liquid formulations while reducing static and improving texture in topical products.
  • UNII 8470G57WFM
    Corn oil is a vegetable oil extracted from corn kernels. It's used in medicines as a solvent to dissolve active ingredients and help the body absorb them, and sometimes as a lubricant in capsules.
  • 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.
  • UNII ND2M416302
    Isopropyl alcohol is a clear liquid solvent derived from petroleum. In medicines, it dissolves active ingredients and other components, helps the product flow smoothly, and aids in sterilization during manufacturing.
  • UNII 0RE8K4LNJS
    Isopropyl myristate is an oily liquid made from coconut or palm oil. It's used in medicines as an emollient and penetration enhancer to help the medicine absorb through skin or improve spreadability in topical products.
  • UNII A2I8C7HI9T
    Methylparaben is a preservative derived from benzoic acid that prevents growth of bacteria, fungi, and mold in medicines. It extends the product's shelf life and maintains safety during storage.
  • 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 1D1K0N0VVC
    A fat-soluble form of vitamin A used as a colorant and nutritional fortification ingredient. It gives products a yellow or orange tint and increases vitamin A content in the formula.
  • 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.

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

The official label also statesWater (Aqua), Isopropyl Alcohol, Glycerin, Acetamidopropyl Trimonium Chloride, Aloe Barbadensis Leaf Juice, C12-15 Alkyl Benzoate, Cocamidopropyl PG-Dimonium Chloride Phosphate, Isopropyl Myristate, Propylene Glycol, Retinyl Palmitate, Tocopheryl Acetate, Zea Mays (Corn) Oil, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum), Methylparaben

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

LabelerGOJO Industries, Inc.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code21749
First marketedFeb 2012
Product typeHuman Otc Drug
Portfolio79 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 10 words ▾

Use Hand sanitizer to help reduce bacteria on the skin

⏱️ Dosage and Administration 20 words ▾

Directions Tear open, unfold and apply to hands Children under 6 years of age should be supervised when using PURELL

⚠️ Warnings 12 words ▾

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

🧪 Active Ingredient 5 words ▾

Active ingredient Ethyl alcohol 62%

🧪 Inactive Ingredients 42 words ▾

Inactive ingredients Water (Aqua), Isopropyl Alcohol, Glycerin, Acetamidopropyl Trimonium Chloride, Aloe Barbadensis Leaf Juice, C12-15 Alkyl Benzoate, Cocamidopropyl PG-Dimonium Chloride Phosphate, Isopropyl Myristate, Propylene Glycol, Retinyl Palmitate, Tocopheryl Acetate, Zea Mays (Corn) Oil, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum), Methylparaben

🎯 Purpose 2 words ▾

Purpose Antimicrobial

📄 When Using This Product 21 words ▾

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

📄 Stop Use and Ask a Doctor If 13 words ▾

Stop use and ask a doctor if irritation or rash appears and lasts

📄 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.

📄 Questions or Comments 12 words ▾

Questions? Call 1-800-321-9647 Monday through Friday 8:30 AM to 5:00 PM www.PURELL.com

📄 Package Label / Principal Display Panel 2 words ▾

Product 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 GOJO Industries, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
GOJO Industries, 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.
← 21749-0363-76 · GOJO 21749-0367-36 · GOJO →
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.