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PURELL Advanced Instant Hand Sanitizer ALCOHOL .7 mL/mL Liquid, 60 mL — NDC 21749-700-60 (Billing 21749-0700-60)

by GOJO Industries, Inc. · 60 mL in 1 BOTTLE

This is a package of 60 mL of PURELL Advanced Instant Hand Sanitizer ALCOHOL .7 mL/mL Liquid from GOJO Industries, Inc., no longer marketed (first marketed May 2011), no longer in the FDA NDC Directory.

NDC 21749-0700-60
🏷️ FDA NDC (as labeled) 21749-700-60 billing pads the product segment with a zero
This package
Contains60 mL Pack sizes19 compare ↓
Product page 21749-0700-00 Also comes in: 1.2 ml 21749-700-00 4 bottles 21749-700-67 4 bottles 21749-700-89 15 ml 21749-700-15 24 bottles 21749-700-02 30 ml 21749-700-01 89 ml 21749-700-03 118 ml 21749-700-04 222 ml 21749-700-07 236 ml 21749-700-08 295 ml 21749-700-29 355 ml 21749-700-12 450 ml 21749-700-45 473 ml 21749-700-47 590 ml 21749-700-59 800 ml 21749-700-80 1000 ml 21749-700-10 2000 ml 21749-700-20
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ 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

⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Jul 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 21749-700-60
Product NDC 21749-700
11-digit billing NDC 21749070060
RxCUI 582753
UNII 3K9958V90M
Application # 505G(a)(3)
SPL Set ID 49bce138-8be2-4bf4-9eeb-f354308cd594
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Jul 2026)
Marketing start 2011-05-10
Route TOPICAL
Dosage form LIQUID
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 582753
Why two NDCs? The FDA registers this code as 21749-700-60 — 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 → 21749-0700-60. 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: 1.2 ml 4 bottles 4 bottles 15 ml 24 bottles 30 ml 89 ml 118 ml 222 ml 236 ml 295 ml 355 ml 450 ml 473 ml 590 ml 800 ml 1000 ml 2000 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
21749-0700-00 21749-700-00 Main listing 1.2 mL in 1 BOTTLE 2016-01-01 — Discontinued by firm
21749-0700-01 21749-700-01 30 mL in 1 BOTTLE 2011-05-10 — Discontinued by firm
21749-0700-02 21749-700-02 24 BOTTLE in 1 CASE / 59 mL in 1 BOTTLE 2011-05-10 — Discontinued by firm
21749-0700-03 21749-700-03 89 mL in 1 BOTTLE 2011-05-10 — Discontinued by firm
21749-0700-04 21749-700-04 118 mL in 1 BOTTLE 2011-05-10 — Discontinued by firm
21749-0700-07 21749-700-07 222 mL in 1 BOTTLE 2011-05-10 — Discontinued by firm
21749-0700-08 21749-700-08 236 mL in 1 BOTTLE 2011-05-10 — Discontinued by firm
21749-0700-10 21749-700-10 8 BAG in 1 CASE / 1000 mL in 1 BAG 2011-05-10 — Discontinued by firm
21749-0700-12 21749-700-12 355 mL in 1 BOTTLE 2011-05-10 — Discontinued by firm
21749-0700-15 21749-700-15 15 mL in 1 BOTTLE 2011-05-10 — Discontinued by firm
21749-0700-20 21749-700-20 4 BAG in 1 CASE / 2000 mL in 1 BAG 2011-05-10 — Discontinued by firm
21749-0700-29 21749-700-29 295 mL in 1 PACKAGE 2017-09-28 — Discontinued by firm
21749-0700-45 21749-700-45 450 mL in 1 PACKAGE 2016-01-01 — Discontinued by firm
21749-0700-47 21749-700-47 473 mL in 1 BOTTLE 2011-05-10 — Discontinued by firm
21749-0700-59 21749-700-59 590 mL in 1 BOTTLE 2011-05-10 — Discontinued by firm
21749-0700-60 You're viewing this 60 mL in 1 BOTTLE 2011-05-10 — Discontinued by firm
21749-0700-67 21749-700-67 4 BOTTLE, PUMP in 1 CASE / 2000 mL in 1 BOTTLE, PUMP 2011-05-10 — Discontinued by firm
21749-0700-80 21749-700-80 800 mL in 1 BOTTLE 2011-05-10 — Discontinued by firm
21749-0700-89 21749-700-89 4 BOTTLE in 1 CASE / 1200 mL in 1 BOTTLE 2011-05-10 — Discontinued by firm

Pack size FAQ

What quantity is in this package?
This package contains 60 mL — 60 ml in 1 bottle.
How does this package differ from NDC 21749-0700-00?
Both are PURELL Advanced Instant Hand Sanitizer ALCOHOL .7 mL/mL Liquid — the drug itself is identical. This page's package is the 60 mL one, while NDC 21749-0700-00 is the 1.2 ml package.
What NDC number is used to bill for this package of PURELL Advanced Instant Hand Sanitizer 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/mLthis 21749-0700-60 GOJO 60 ml — — Discontinued —
PURELL Waterless Surgical Scrub .7 mL/mL 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
May 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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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 marketedMay 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
🎯 Indications and Usage 14 words ▾

Use Hand sanitizer to help reduce bacteria on the skin that could cause disease

⏱️ Dosage and Administration 31 words ▾

Directions Place enough product in your palm to thoroughly cover your hands Rub hands together briskly until dry Children under 6 years of age should be supervised when using this product

⚠️ Warnings 65 words ▾

Warnings Flammable. Keep away from fire or flame. For external use only 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 irritation or rash appears and lasts Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 5 words ▾

Active ingredient Ethyl alcohol 70%

🧪 Inactive Ingredients 21 words ▾

Inactive ingredients Water (Aqua), Isopropyl Alcohol, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum)

🎯 Purpose 2 words ▾

Purpose Antimicrobial

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 No longer marketed (per FDA listing data)
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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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.
Does this product come in other package sizes?
Yes — the FDA directory lists 18 other package presentations of this same product, including 1.2 ml (21749-0700-00), 4 bottles (21749-0700-67), 4 bottles (21749-0700-89). 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.
← 21749-0687-40 · GOJO 21749-0702-08 · 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.