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PURELL Waterless Surgical Scrub alcohol .7 mL/mL Liquid, 59 mL — NDC 21749-0992-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

PURELL Waterless Surgical Scrub alcohol .7 mL/mL Liquid, 59 mL — NDC 21749-992-02 (Billing 21749-0992-02)

by GOJO Industries, Inc. · 59 mL in 1 BOTTLE

This is a package of 59 mL of PURELL Waterless Surgical Scrub alcohol .7 mL/mL Liquid from GOJO Industries, Inc., marketed since Dec 2011 and currently FDA-listed. It is the main listing for this product, which comes in 3 package sizes.

NDC 21749-0992-02
🏷️ FDA NDC (as labeled) 21749-992-02 billing pads the product segment with a zero
This package
Contains59 mL Pack sizes3 compare ↓
Main listing for product 21749-992 · Also comes in: 1000 ml 21749-992-33 1200 ml 21749-992-89
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) 21749-992-02
Product NDC 21749-992
11-digit billing NDC 21749099202
RxCUI 582753
UNII 3K9958V90M
Application # 505G(a)(3)
SPL Set ID e3ed5e0c-1e21-47eb-a999-9c8aa5083dff
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2011-12-15
Route TOPICAL
Dosage form LIQUID
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 582753
Why two NDCs? The FDA registers this code as 21749-992-02 — 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 → 21749-0992-02. 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.
Try another pack size: 1000 ml 1200 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
21749-0992-02 You're viewing this Main listing 59 mL in 1 BOTTLE 2011-12-15 — Active
21749-0992-33 21749-992-33 1000 mL in 1 BOTTLE 2011-12-15 — Discontinued by firm
21749-0992-89 21749-992-89 1200 mL in 1 BOTTLE 2011-12-15 — Active

You're viewing the smallest of 3 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 59 mL — 59 ml in 1 bottle.
How does this package differ from NDC 21749-0992-33?
Both are PURELL Waterless Surgical Scrub alcohol .7 mL/mL Liquid — the drug itself is identical. This page's package is the 59 mL one, while NDC 21749-0992-33 is the 1000 ml package.
What NDC number is used to bill for this package of PURELL Waterless Surgical Scrub alcohol .7 mL/mL 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
Ethyl Rubbing Alcohol 70 mL/100mL 70000-0020-01 Cardinal 473 ml $0.004 — Availability likely —
Ethyl alcohol 70 mL/100mL 70677-1220-01 Strategic 473 ml $0.004 — Availability likely —
Ethyl Rubbing Alcohol 70 mL/100mL 00363-0876-43 Walgreen 473 ml — — FDA listed —
Ethyl Rubbing Alcohol 700 mg/mL 00395-0040-16 Humco 473 ml — — FDA listed —
Rubbing 70 mL/100mL 00869-0876-43 Nice-Pak 473 ml — — FDA listed —
Alcare Antiseptic Handrub 70 mL/100mL 11084-0035-18 SC 370 ml — — FDA listed —
Ethyl Alcohol 70 mL/100mL 11344-0876-43 Nice-Pak 473 ml — — FDA listed —
Signature Select Advanced Hand Sanitizer with Aloe Vera 70 mL/100mL 21130-0066-01 Living 59 ml — — FDA listed —
Signature Select Advanced Hand Sanitizer 70 mL/100mL 21130-0077-01 Living 59 ml — — FDA listed —
PURELL Advanced Instant Hand Sanitizer .7 mL/mL 21749-0700-00 GOJO 1.2 ml — — Discontinued —
PURELL Waterless Surgical Scrub .7 mL/mLthis 21749-0992-02 GOJO 59 ml — — FDA listed —
Rubbing 70 mL/100mL 41163-0876-43 United 473 ml — — FDA listed —
Rubbing 70 mL/100mL 50804-0876-43 Perrigo 473 ml — — FDA listed —
DOP Ethyl Alcohol 70% 70 mL/100mL 51048-0048-16 Omega 473 ml — — FDA listed —
INSTANT HAND SANITIZER Classic 70 mL/100mL 52000-0434-01 Universal 1000 ml — — FDA listed —
Ethyl Rubbing Alcohol 70 mL/100mL 55301-0876-43 Your 473 ml — — FDA listed —
Hand sanitizer 8oz with vitamin E 70 mL/100mL 55319-0116-01 Midwood 236 ml — — FDA listed —
Hand sanitizer 8oz with aloe vera 70 mL/100mL 55319-0117-01 Midwood 236 ml — — FDA listed —
Hand sanitizer 16.9oz with vitamin E 70 mL/100mL 55319-0118-01 Midwood 500 ml — — FDA listed —
Instant Hand Sanitizer 2oz Bonus pack 70 mL/100mL 57337-0093-01 Rejoice 59 ml — — FDA listed —
Hand Sanitizer w/ Carabiner (Strawberry Scented) 2oz Bonus pack 70 mL/100mL 57337-0094-01 Rejoice 2 bottles — — FDA listed —
Hand Sanitizer w/ Carabiner (Lemon Scented) 2oz Bonus pack 70 mL/100mL 57337-0095-01 Rejoice 2 bottles — — FDA listed —
Hand Sanitizer w/ Carabiner (Watermelon Scented) 2oz Bonus pack 70 mL/100mL 57337-0096-01 Rejoice 2 bottles — — FDA listed —
Hand Sanitizer 1.8 oz Antiseptic 70 mL/100mL 57337-0107-01 REJOICE 1 bottle — — FDA listed —
Hand Sanitizer 1.8 oz Lemon Ice 70 mL/100mL 57337-0110-01 Ningbo 53 ml — — FDA listed —
Hand Sanitizer 1.8 oz Watermelon Scented 1.8 oz. 70 mL/100mL 57337-0111-01 Ningbo 53 ml — — FDA listed —
Hand Sanitizer 1.8 oz Strawberry Scented 70 mL/100mL 57337-0112-01 Ningbo 53 ml — — FDA listed —
Hand Sanitizer Vitamin E and Aloe Vera 2 oz. 2 pk 70 mL/100mL 57337-0114-01 Ningbo 2 bottles — — FDA listed —
Hand Sanitizer 8 oz. Vitamin E 70 v/v 70 mL/100mL 57337-0115-01 Ningbo 236 ml — — FDA listed —
Hand Sanitizer Vitamin E and Aloe Vera 70 mL/100mL 57337-0116-01 Ningbo 236 ml — — FDA listed —
Hand Sanitizer Original 1.8 oz 70 mL/100mL 57337-0117-01 Ningbo 53 ml — — FDA listed —
Hand Sanitizer Antibacterial Vitamin E 2 oz. 2 pk 70 mL/100mL 57337-0118-01 Ningbo 2 bottles — — FDA listed —
Hand Sanitizer Vitamin E 70 mL/100mL 57337-0119-01 Ningbo 2 bottles — — FDA listed —
Hand Sanitizer Antibacterial Vitamin E 70 mL/100mL 57337-0120-01 Ningbo 500 ml — — FDA listed —
Hand Sanitizer Antibacterial Vitamin E 70 mL/100mL 57337-0121-01 Ningbo 177 ml — — FDA listed —
Hand Sanitizer Antibacterial Vitamin E 70 mL/100mL 57337-0122-01 Ningbo 1000 ml — — FDA listed —
Hand Sanitizer 2pk Lemon 2oz 70 mL/100mL 57337-0123-01 Ningbo 1 bottle — — FDA listed —
Hand Sanitizer Original 8oz 70 mL/100mL 57337-0124-01 Ningbo 236 ml — — FDA listed —
Hand Sanitizer with Clip 1.8oz 70 mL/100mL 57337-0125-01 Ningbo 1 bottle — — FDA listed —
Hand Sanitizer 2pk Aloe 2oz 70 mL/100mL 57337-0126-01 Ningbo 1 bottle — — FDA listed —
Hand Sanitizer Aloe 2oz 70 mL/100mL 57337-0127-01 Ningbo 59 ml — — FDA listed —
Hand Sanitizer 2pk Lavender 2oz 70 mL/100mL 57337-0128-01 Ningbo 1 bottle — — FDA listed —
Hand Sanitizer Lavender 2oz 70 mL/100mL 57337-0129-01 Ningbo 59 ml — — FDA listed —
Hand Sanitizer Pouch 70 mL/100mL 57337-0130-01 Ningbo 2.1 ml — — FDA listed —
Hand Sanitizer 24ct Pouch 70 mL/100mL 57337-0131-01 Ningbo 1 pouch — — FDA listed —
Hand Sanitizer Lemon 2oz 70 mL/100mL 57337-0133-01 Ningbo 59 ml — — FDA listed —
Hand Sanitizer Aloe 8oz 70 mL/100mL 57337-0134-01 Ningbo 236 ml — — FDA listed —
Hand sanitizer 8oz with vitamin E 70 mL/100mL 57337-0140-01 REJOICE 236 ml — — FDA listed —
Hand sanitizer 8oz with aloe vera 70 mL/100mL 57337-0141-01 REJOICE 236 ml — — FDA listed —
Hand sanitizer 16.9oz with vitamin E 70 mL/100mL 57337-0142-01 REJOICE 500 ml — — FDA listed —
Ethyl Rubbing Alcohol 70 mL/100mL 59779-0164-43 CVS 473 ml — — FDA listed —
CSI E3 Hand Sanitizer 70 mL/100mL 62654-0139-01 Central 3785 ml — — FDA listed —
DD Mart Hand Sanitizer 70 mL/100mL 63148-0114-08 Apollo 236 ml — — FDA listed —
HiGHMARK 70 mL/100mL 63148-0402-08 Apollo 236 ml — — FDA listed —
Himark 70 mL/100mL 63148-0403-08 Apollo 236 ml — — FDA listed —
Instant Antiseptic Hand Sanitizer 70 mL/100mL 63998-0364-01 United 750 ml — — FDA listed —
Skinsei 700 mg/mL 64942-1740-01 Conopco 118 ml — — FDA listed —
CoreTex Antibacterial Hand Sanitizer 70 mL/100mL 65753-0201-01 CoreTex 30 ml — — FDA listed —
Germ Attack Hand Sanitizer .7 mL/mL 66902-0482-02 Natural 59 ml — — FDA listed —
Handy Solutions Hand Sanitizer 70 mL/100mL 67751-0086-01 Navajo 59 ml — — FDA listed —
Alcohol 70 mL/100mL 68196-0602-68 Sam's 2000 ml — — FDA listed —
Zoono Ultra Hand Sanitizer 70 g/100mL 69221-0501-01 Zoono 150 ml — — FDA listed —
Sierra Soft Alcohol Hand Sanitizer 700 mg/mL 70415-0100-01 CWGC 1000 ml — — FDA listed —
Ethyl Rubbing Alcohol 70 mL/100mL 70677-0056-01 STRATEGIC 473 ml — — Discontinued —
Bluesea Instant Hand Sanitizer 70 mL/100mL 72119-0003-01 BLUE 60 ml — — FDA listed —
Ethyl Rubbing Alcohol 70 mL/100mL 72288-0876-43 Amazon.com 473 ml — — FDA listed —
KONIX Alcohol Antiseptic Hand Rub 70 mL/100mL 73107-0105-30 TURKUAZ 30 ml — — FDA listed —
Noshinku Eucalyptus Hand Sanitizer 70 mL/100mL 73898-0002-20 Noshinku 20 ml — — FDA listed —
Noshinku Lavender Hand Sanitizer 70 mL/100mL 73898-0003-20 Noshinku 20 ml — — FDA listed —
Nourishing Hand Sanitizer Orange Coriander 70 mL/100mL 73898-0008-02 Noshinku 3800 ml — — FDA listed —
Hand Sanitizer Vanilla Creme 70 mL/100mL 73898-0009-20 Noshinku 20 ml — — FDA listed —
Hand Sanitizer Pear Blossom Tea 70 mL/100mL 73898-0010-20 Noshinku 20 ml — — FDA listed —
Hand Sanitizer Santal Blanc 70 mL/100mL 73898-0011-20 Noshinku 20 ml — — FDA listed —
Fresh Feels Hand Sanitizer Mist 70 mL/100mL 73905-0045-01 ZHEJIANG 40 ml — — FDA listed —
EcoChoice Sterno Hand Sanitizer Lemon Zest 70 mL/100mL 73926-0753-01 STERNO 2 ml — — FDA listed —
EcoChoice Sterno Hand Sanitizer Clean and Fresh 70 mL/100mL 73926-0754-01 STERNO 59 ml — — FDA listed —
70 Alcohol Hand Sanitizer 70 mL/100mL 74375-0060-01 Iron 355 ml — — FDA listed —
Signature Care Advanced Hand Sanitizer with Aloe 70 mL/100mL 75262-0006-01 ZheJiang 59 ml — — Discontinued —
Instant Hand Sanitizer 70 mL/100mL 75541-0016-01 NINGBO 236 ml — — FDA listed —
Hand sanitizer 8oz with vitamin E 70 mL/100mL 75742-0019-01 Zhejiang 236 ml — — FDA listed —
Hand sanitizer 8oz with aloe vera 70 mL/100mL 75742-0020-01 Zhejiang 236 ml — — FDA listed —
Hand sanitizer 16.9oz with vitamin E 70 mL/100mL 75742-0021-01 Zhejiang 500 ml — — FDA listed —
Hand sanitizer 16.9oz with vitamin E 70 mL/100mL 75742-0029-01 Zhejiang 500 ml — — FDA listed —
Hand sanitizer 8oz with aloe vera 70 mL/100mL 75742-0030-01 Zhejiang 236 ml — — FDA listed —
Hand sanitizer 8oz with vitamin E 70 mL/100mL 75742-0031-01 Zhejiang 236 ml — — FDA listed —
Mellow Hand Sanitizer Aloe 70 mL/100mL 77725-0005-17 L.e.d. 500 ml — — FDA listed —
Ethyl Alcohol 70 mL/100mL 79903-0283-16 Walmart 473 ml — — FDA listed —
DOCTORS TOUCH Hand Sanitizer 70 mL/100mL 80045-0313-00 DOCTOR'S 59 ml — — FDA listed —
b pure Hydrating Hand Sanitizer Vanilla Sugar Cookie Scented 70 mL/100mL 80684-0112-00 FOURSTAR 30 ml — — FDA listed —
b pure Hydrating Hand Sanitizer Frosted Coconut Scented 70 mL/100mL 80684-0113-00 FOURSTAR 30 ml — — FDA listed —
Aloe Scented Hand Sanitizer 70 mL/100mL 80684-0120-00 FOURSTAR 89 ml — — FDA listed —
Eucalyptus Scented Hand Sanitizer 70 mL/100mL 80684-0121-00 FOURSTAR 89 ml — — FDA listed —
Shea Butter Scented Hand Sanitizer 70 mL/100mL 80684-0122-00 FOURSTAR 89 ml — — FDA listed —
B Pure Moisturizing Hand Sanitizer Poppy Scented 70 mL/100mL 80684-0130-00 Fourstar 34 ml — — FDA listed —
B Pure Moisturizing Hand Sanitizer Rainbow Sherbert Scented 70 mL/100mL 80684-0131-00 Fourstar 34 ml — — FDA listed —
B-Pure Moisturizing Hand Sanitizer Honey Crisp Apple Scented 70 mg/100mL 80684-0156-00 FOURSTAR 34 ml — — FDA listed —
B-Pure Moisturizing Hand Sanitizer Pumpkin Vanilla Scented 70 mg/100mL 80684-0157-00 FOURSTAR 34 ml — — FDA listed —
Ethyl Rubbing Alcohol 70 Percent 700 mg/mL 82645-0926-16 Pharma 473 ml — — FDA listed —
Advanced Hand Sanitizer 70 mL/100mL 83324-0065-02 Chain 59 ml — — FDA listed —
Zoviro 70 mL/100mL 83814-0005-01 Zoviro, 60 ml — — FDA listed —
VQ Hydrating Hand Sanitizer Fresh Watermelon 70 mL/100mL 85980-0001-01 Tychea 30 ml — — FDA listed —
VQ Hydrating Hand Sanitizer Violet Vanilla 70 mL/100mL 85980-0002-01 Tychea 30 ml — — FDA listed —
VQ Hydrating Hand Sanitizer Caramel Pistachio 70 mL/100mL 85980-0003-01 Tychea 1 bottle — — FDA listed —
VQ Hydrating Hand Sanitizer Coconut 70 mL/100mL 85980-0004-01 Tychea 1 bottle — — FDA listed —
VQ Hydrating Hand Sanitizer Pink Dragon Fruit 70 mL/100mL 85980-0005-01 Tychea 1 bottle — — FDA listed —
VQ Hydrating Hand Sanitizer Rose Lychee 70 mL/100mL 85980-0006-01 Tychea 1 bottle — — FDA listed —
VQ Hydrating Hand Sanitizer Sugar Plum 70 mL/100mL 85980-0007-01 Tychea 1 bottle — — FDA listed —
Recens Foam .7 mL/mL 75990-0968-07 Certus 700 ml — — Discontinued —
PURELL Advanced Hand Sanitizer Fragrance Free .7 mL/mL 21749-0532-01 GOJO 1.2 ml — — FDA listed —
Fast .7 mL/mL 62257-0658-08 ABC 1000 ml — — Discontinued —
PURELL Healthcare Advanced Hand Sanitizer Foam .7 mL/mL 21749-0811-45 GOJO 450 ml — — Discontinued —
Lynx san a foam .7 mL/mL 62257-0007-10 ABC 1000 ml — — FDA listed —
EXTENDED CARE Foaming Hand Sanitizer .7 mL/mL 71875-0800-40 TRIPLE 1200 ml — — FDA listed —
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 Healthcare Advanced Hand Sanitizer Gentle and Free Foam .7 mL/mL 21749-0822-53 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 Gentle and Free Foam .7 mL/mL 21749-0826-53 GOJO 535 ml — — FDA listed —
Sani-Spritz .7 mL/mL 62257-0738-15 ABC 946 ml — — FDA listed —
PURELL Advanced Hand Sanitizer Biobased Content .7 mL/mL 21749-0022-02 GOJO 60 ml — — FDA listed —
Hand San .7 mL/mL 59503-2605-01 Rochester 472 ml — — Discontinued —
PURELL Healthcare Advanced Hand Sanitizer ULTRA NOURISHING Foam .7 mL/mL 21749-0854-53 GOJO 535 ml — — FDA listed —
PURELL Advanced Instant Hand Sanitizer .7 mL/mL 21749-0807-17 GOJO 515 ml — — FDA listed —
PURELL Advanced Hand Sanitizer Green Certified Foam .7 mL/mL 21749-0808-51 GOJO 550 ml — — FDA listed —
PURELL Advanced Hand Sanitizer Gel .7 mL/mL 21749-0709-45 GOJO 450 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

🏛️
2011
On the market since
Dec 2011
📍
2026
Currently FDA-listed
15 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 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 J8T3X564IH
    A clear oily liquid derived from sebacic acid, used as a plasticizer and solvent in pharmaceutical coatings and films to improve flexibility and help active ingredients dissolve properly.
  • 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 RFW2ET671P
    Hydroxypropyl cellulose is a plant-derived thickening agent made from cellulose. It acts as a binder to hold tablet ingredients together and as a film-former to coat tablets or control how fast the medicine releases.
  • 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 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 255PIF62MS
    A synthetic antioxidant compound used to prevent oils and fats in medications from breaking down or becoming rancid during storage. It helps maintain the medicine's stability and shelf life.
  • 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.

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

The official label also statesWater (Aqua), Isopropyl Myristate, Glycerin, Diisopropyl Sebacate, Citric Acid, PEG/PPG-20/6 Dimethicone, Tetradibutyl Pentaerythrityl Hydroxyhydrocinnamate, Hydroxypropylcellulose, Polyquaternium-37, Methylchloroisothiazolinone, Methylisothiazolinone

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 marketedDec 2011
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 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 18 words ▾

Uses Significantly reduces the number of micro-organisms on the hands and forearms prior to surgery or patient care

⏱️ Dosage and Administration 81 words ▾

Directions clean under the nails with a nail pick mails should be maintained with a 1 millimeter free edge place 2 mL of product into palm of one hand dip fingers of opposite hand into the product and work under nails spread remaining product evenly over the hands and lower 2/3 of one forearm paying particular attention to the nails, cuticles, and interdigital spaces place 2 mL of product into opposite hand and repeat steps above allow to air dry completely

⚠️ Warnings 97 words ▾

Warnings Flammable. Keep away from fire or flame. For external use only Sunburn Alert: This product contains an alpha hydroxy acid (AHA) that may increase the risk of sunburn.

Take steps to limit sun exposure while using this product and for one week following use. Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation and redness develop and persist 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 Ethyl alcohol 70% v/v

🧪 Inactive Ingredients 20 words ▾

Inactive ingredients Water (Aqua), Isopropyl Myristate, Glycerin, Diisopropyl Sebacate, Citric Acid, PEG/PPG-20/6 Dimethicone, Tetradibutyl Pentaerythrityl Hydroxyhydrocinnamate, Hydroxypropylcellulose, Polyquaternium-37, Methylchloroisothiazolinone, Methylisothiazolinone

🎯 Purpose 5 words ▾

Purpose Antiseptic surgical hand scrub

📄 When Using This Product 15 words ▾

Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.

📄 Stop Use and Ask a Doctor If 18 words ▾

Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

📄 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.

📄 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 ↗

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 PURELL Waterless Surgical Scrub (this brand).

Top reported reactions

Toxicity To Various Agents6,004
Completed Suicide5,433
Drug Abuse5,289
Overdose1,888
Death1,594
Intentional Overdose1,540
Cardio-respiratory Arrest1,346

Age at onset

Neonate26
Infant14
Child16
Adolescent92
Adult2,810
Elderly294

Reporter sex

26,727 reports
Male · 55%
Female · 45%
Unknown · 0%

Serious outcomes

Hospitalization8,618
Reports over time (by year) — tap or hover for the count & year
2021 2022 2024 2026 2,567 1,499
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 GOJO Industries, 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 2 other package presentations of this same product, including 1000 ml (21749-0992-33), 1200 ml (21749-0992-89). 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?
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.
← 21749-0975-04 · GOJO 21749-0994-02 · 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.