Home › NDC Lookup › Ingredients › Benzalkonium Chloride › 72119-0004-01
U HAND SANITIZER CLASSIC BENZALKONIUM CHLORIDE .13 g/100mL Solution, 100 mL — NDC 72119-0004-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

U HAND SANITIZER CLASSIC BENZALKONIUM CHLORIDE .13 g/100mL Solution, 100 mL — NDC 72119-004-01 (Billing 72119-0004-01)

by BLUE SEA AEROSOL & DAILY CARE CO., LTD · 100 mL in 1 BOTTLE

This is a package of 100 mL of U HAND SANITIZER CLASSIC BENZALKONIUM CHLORIDE .13 g/100mL Solution from BLUE SEA AEROSOL & DAILY CARE CO., LTD, marketed since Jun 2020 and currently FDA-listed. It is the main listing for this product, which comes in 3 package sizes.

NDC 72119-0004-01
🏷️ FDA NDC (as labeled) 72119-004-01 billing pads the product segment with a zero
This package
Contains100 mL Pack sizes3 compare ↓
Main listing for product 72119-004 · Also comes in: 200 ml 72119-004-02 473 ml 72119-004-03
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

NDC database record

One package, one record: these facts belong to NDC 72119-004-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
72119 labeler · 004 product · 01 package
Package marketed since
Jun 19, 2020
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0676979556321
FDA record last changed
Jul 24, 2026
⚠️
Other active recalls for Benzalkonium Chloride (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Apr 8, 2026 — CGMP Deviations: product manufactured in the same facility under the same conditions as the product found to be contaminated (Blaine Labs Inc) · FDA recall D-0693-2026
Class II · Apr 8, 2026 — CGMP Deviations; product manufactured in the same facility under the same conditions as the product found to be contaminated (Blaine Labs Inc) · FDA recall D-0699-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0375-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0369-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0365-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0374-2026
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) 72119-004-01
Product NDC 72119-004
11-digit billing NDC 72119000401
RxCUI 1049254
UNII F5UM2KM3W7
UPC 0676979556321
Application # M005
SPL Set ID fbc27a24-0e81-4907-b24f-881c4fe0ec44
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-06-19
Route TOPICAL
Dosage form SOLUTION
Substance BENZALKONIUM CHLORIDE
Quick answers
  • RxCUI (RxNorm): 1049254
Why two NDCs? The FDA registers this code as 72119-004-01 — 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 → 72119-0004-01. 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 Quaternary ammonium compounds class.

Drug family (ATC) Quaternary ammonium compounds, Medicated dressings with antiinfectives, Antiseptics
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

🧪 What is this product?

This is an over-the-counter topical solution hand sanitizer containing benzalkonium chloride at 0.13 g per 100 mL. Benzalkonium chloride is an antimicrobial agent typically used in sanitizing products to reduce bacteria and other germs on the skin. This product is marketed as an OTC monograph drug, meaning it follows FDA's established rules for hand sanitizer ingredients rather than being individually reviewed as a new drug application.

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: 200 ml 473 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
72119-0004-01 You're viewing this Main listing 100 mL in 1 BOTTLE 2020-06-19 — Active
72119-0004-02 72119-004-02 200 mL in 1 BOTTLE 2020-06-19 — Active
72119-0004-03 72119-004-03 473 mL in 1 BOTTLE 2020-06-19 — 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 100 mL — 100 ml in 1 bottle.
How does this package differ from NDC 72119-0004-02?
Both are U HAND SANITIZER CLASSIC BENZALKONIUM CHLORIDE .13 g/100mL Solution — the drug itself is identical. This page's package is the 100 mL one, while NDC 72119-0004-02 is the 200 ml package.
What NDC number is used to bill for this package of U HAND SANITIZER CLASSIC BENZALKONIUM CHLORIDE .13 g/100mL Solution?
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
Walgreens Advanced Wound Wash 1.3 mg/mL 00363-9656-10 Walgreens 1 bottle — — FDA listed —
HUMCO Merthiolate 1.3 mg/mL 00395-8010-92 Humco 59 ml — — FDA listed —
Bak 1 750 .1713 g/100mL 12745-0145-01 Medical 473 ml — — FDA listed —
Tincture Merthiolate 1.3 mg/mL 24286-1532-07 DLC 30 ml — — FDA listed —
Puri-San Plus Instant Hand Sanitizer 1.3 mg/mL 43097-0457-10 People's 1000 ml — — Discontinued —
United Airlines .13 g/100mL 52305-0601-25 Freshorize 250 ml — — FDA listed —
Alaska Airlines .13 g/100mL 52305-0602-30 Freshorize 250 ml — — FDA listed —
El Valle Merthiolate 1.3 mg/mL 55758-0375-02 Pharmadel 30 ml — — FDA listed —
safeHands Hand Sanitizer Fragrance Free .13 g/100mL 60867-0150-02 Safehands 52 ml — — FDA listed —
safeHands Hand Sanitizer Clean Linen .13 g/100mL 60867-0152-02 Safehands 52 ml — — FDA listed —
QS Plus Plus Instant Hand Sanitizer 1.3 mg/mL 62257-0457-10 ABC 1000 ml — — Discontinued —
RELEEV Cold Sore Treatment 1.3 mg/mL 63287-0419-01 Merix 1 pouch — — FDA listed —
Quality Choice Merthiolate 1.3 mg/mL 63868-0493-02 Chain 59 ml — — FDA listed —
Soft Care Instant Hand Sanitizer AF .13 g/100mL 64536-3628-03 Diversey, 1300 ml — — FDA listed —
Bactine Max .13 g/100mL 65197-0820-80 WellSpring 1 bottle — — FDA listed —
Cold Sore Treatment, 24-7 Life by 7-Eleven 1.3 mg/mL 66715-5189-00 Lil' 1 bottle — — FDA listed —
Novex Hand Sanitizer 1.3 mg/mL 66902-0037-25 Natural 225 ml — — FDA listed —
Chemcor Chemical Foaming Hand Sanitizer .0013 mg/mL 68041-0519-00 Chemcor 4 bottles — — FDA listed —
Antimicrobial 1.3 ug/mg 68599-0214-04 McKesson 118 mg — — FDA listed —
Zoono Hand Sanitizer .13 g/100mL 69221-0203-11 Zoono 50 ml — — FDA listed —
Zoono Alcohol Free Hand Sanitizer .13 g/100mL 69221-0601-11 Zoono 50 ml — — FDA listed —
CVS Merthiolate 1.3 mg/mL 69842-0749-92 CVS 59 ml — — FDA listed —
ElimiShield Home and Outdoor Moisturizing Hand Sanitizer 1.3 mg/mL 71853-0006-01 Bryson 50 ml — — FDA listed —
U Hand Sanitizer Classic .13 g/100mLthis 72119-0004-01 BLUE 100 ml — — FDA listed —
Mercurochrome First Aid Antiseptic 1.3 mg/mL 73635-1223-01 Germa 30 ml — — Discontinued —
Merthiolate Tincture First Aid Antiseptic 1.3 mg/mL 73635-1224-01 Germa 30 ml — — Discontinued —
tazza HAND SANITIZER .13 g/.1L 76370-0032-00 Tazza 3.78 l — — FDA listed —
tazza Alcohol-Free sanitizer .13 g/.1L 76370-0041-00 Tazza 1 l — — FDA listed —
Hygiene Clean Clean Cotton Hand Sanitizer 1.3 mg/mL 80499-0001-01 USA 237 ml — — FDA listed —
Hygiene Clean Eucalyptus Hand Sanitizer 1.3 mg/mL 80499-0002-01 USA 237 ml — — FDA listed —
Hygiene Clean Unscented Hand Sanitizer 1.3 mg/mL 80499-0003-01 USA 237 ml — — FDA listed —
Hygiene Clean Pumpkin Spice Hand Sanitizer 1.3 mg/mL 80499-0008-01 USA 50 ml — — FDA listed —
Hygiene Clean Blueberry Lemonade Hand Sanitizer 1.3 mg/mL 80499-0009-01 USA 50 ml — — FDA listed —
Hygiene Clean Leather Oak Hand Sanitizer 1.3 mg/mL 80499-0010-01 USA 50 ml — — FDA listed —
Hygiene Clean Mahogany Teakwood Hand Sanitizer 1.3 mg/mL 80499-0011-01 USA 50 ml — — FDA listed —
Hygiene Clean Bubble Gum Hand Sanitizer 1.3 mg/mL 80499-0012-01 USA 50 ml — — FDA listed —
Hygiene Clean Eucalyptus Hand Sanitizer 1.3 mg/mL 80499-0013-01 USA 50 ml — — FDA listed —
Hygiene Clean Unscented Clean Hand Sanitizer 1.3 mg/mL 80499-0014-01 USA 50 ml — — FDA listed —
Hygiene Clean Balsam Fir Hand Sanitizer 1.3 mg/mL 80499-0015-01 USA 50 ml — — FDA listed —
Hygiene Clean Blueberry Lemonade Hand Sanitizer Car Safe Alcohol-Free 1.3 mg/mL 80499-0017-00 USA 237 ml — — FDA listed —
Hygiene Clean Vanilla Woods Hand Sanitizer Car Safe Alcohol Free 1.3 mg/mL 80499-0018-00 USA 237 ml — — FDA listed —
Hygiene Clean Vanilla Sugar Hand Sanitizer on the go and car safe 1.3 mg/mL 80499-0030-01 USA 50 ml — — FDA listed —
Hygiene Clean Luxury Clean hand Sanitizer on the go and car safe 1.3 mg/mL 80499-0031-01 USA 50 ml — — FDA listed —
Hygiene Clean Lavender Blossom Hand Sanitizer 1.3 mg/mL 80499-0103-01 USA 50 ml — — FDA listed —
Hygiene Clean Lilac Garden Hand Sanitizer 1.3 mg/mL 80499-0104-01 USA 50 ml — — FDA listed —
Hygiene Clean Spring Bloom Hand Sanitizer 1.3 mg/mL 80499-0105-01 USA 50 ml — — FDA listed —
Purifi Hand Sanitizer .13 g/100mL 80659-0301-01 Purifi 250 ml — — FDA listed —
Merthiolate 1.3 mg/mL 82645-0912-92 Pharma 59 ml — — FDA listed —
Caseys .13 g/100g 85844-0001-01 Zhejiang 15 patches — — FDA listed —
Refresh Sanitizing Towlette Organic Grapefruit Splash .13 g/100mL 45942-1629-02 GIOVANNI 24 packets — — FDA listed —
Recharge Sanitizing Towlette Organic Peppermint Surge .13 g/100mL 45942-1630-02 GIOVANNI 24 packets — — FDA listed —
Relax Sanitizing Towlette Organic Lavender Calm .13 g/100mL 45942-1631-02 GIOVANNI 24 packets — — FDA listed —
Soft Care Sentry .13 g/100mL 64536-1948-03 Diversey, 1300 ml — — FDA listed —
Antibacterial Hand Blueberries .13 g/100mL 76176-0046-01 NINGBO 400 ml — — FDA listed —
Antibacterial Hand Cucumber And Tea Tree .13 g/100mL 76176-0047-01 NINGBO 400 ml — — FDA listed —
Global Care Gold Antibacterial Hand .13 g/100mL 76176-0159-01 NINGBO 400 ml — — FDA listed —
Antibacterial Berry Medley .13 g/100mL 52000-0436-64 Universal 1893 ml — — FDA listed —
Dial Foaming Antibacterial Defense Hand Wash Apple Burst .13 g/100mL 54340-0001-02 Henkel 6 bottles — — FDA listed —
Dial Foaming Antibacterial Sensitive Fragrance Free .13 g/100mL 54340-0194-01 Henkel 221 ml — — FDA listed —
Zep Acclaim AB .13 g/100mL 66949-0114-24 Zep 15140 ml — — FDA listed —
Zep Acclaim AB .13 g/100mL 66949-0131-01 Zep 11400 ml — — FDA listed —
Appeal Antibacterial Hand Wash .13 g/100mL 11084-0015-27 SC 1000 ml — — FDA listed —
Instant Foam Non-alcohol PURE Hand Sanitizer .13 g/100mL 11084-0300-01 SC 47 ml — — Discontinued —
Antibacterial Handwash Lavender Bouquet .13 g/100mL 52000-0042-01 Universal 400 ml — — FDA listed —
Antibacterial Handwash Blueberries .13 g/100mL 52000-0047-01 Universal 400 ml — — FDA listed —
Antibacterial Lavender Bouquet .13 g/100mL 52000-0435-64 Universal 1893 ml — — FDA listed —
Dial Antibacterial Hydrating Shea Butter .13 g/100mL 54340-0015-02 Henkel 12 bottles — — FDA listed —
Dial Antibacterial Defense Orchid Rose Bliss Scent .13 g/100mL 54340-0131-01 Henkel 12 bottles — — FDA listed —
Dial Foaming Antibacterial Defense Soothing White Tea .13 g/100mL 54340-0186-01 Henkel 221 ml — — FDA listed —
Dial Foaming Antibacterial Defense Spring Water .13 g/100mL 54340-0195-01 Henkel 221 ml — — FDA listed —
Zep Fuzion FS Antimicrobial Foaming Hand Cleaner .13 g/100mL 66949-0132-17 Zep 4800 ml — — FDA listed —
Ormadus Foodservice Antibacterial Foam .13 g/100mL 11084-0023-66 SC 1000 ml — — FDA listed —
Antibacterial Handwash Berry Medley .13 g/100mL 52000-0044-01 Universal 400 ml — — FDA listed —
Dial Antibacterial Chestnut Bliss Limited Seasonal .13 g/100mL 54340-0008-02 Henkel 12 bottles — — FDA listed —
Dial Antibacterial Citrus Sorbet Limited Seasonal .13 g/100mL 54340-0012-02 Henkel 12 bottles — — FDA listed —
Dial Antibacterial Defense Gold .13 g/100mL 54340-0173-01 Henkel 325 ml — — FDA listed —
Dial Foaming Antibacterial Sensitive Aloe .13 g/100mL 54340-0193-01 Henkel 221 ml — — FDA listed —
SYMMETRY ANTIMICROBIAL FOAMING HAND WASH w/Benzalkonium Chloride .13 g/100mL 30805-0017-02 Buckeye 1250 ml — — FDA listed —
Dial Antibacterial Defense Sandalwood Vanilla .13 g/100mL 54340-0133-01 Henkel 12 bottles — — FDA listed —
Dial Antibacterial Defense Spring Water .13 g/100mL 54340-0183-01 Henkel 325 ml — — FDA listed —
Dial Foaming Antibacterial Defense Citrus Sunburst .13 g/100mL 54340-0188-01 Henkel 221 ml — — FDA listed —
Zep Professional Mild AB .13 g/100mL 66949-0130-06 Zep 6000 ml — — FDA listed —
Zep Pear Ab Hs .13 g/100mL 66949-0393-01 Zep 6000 ml — — FDA listed —
Dial Professional Antibacterial Defense Spring Water .13 g/100mL 54340-0121-02 Henkel 4 bottles — — FDA listed —
Dial Antibacterial Defense Lavender and Jasmine .13 g/100mL 54340-0175-01 Henkel 325 ml — — FDA listed —
Dial Foaming Antibacterial Defense Fresh Pear .13 g/100mL 54340-0185-01 Henkel 221 ml — — FDA listed —
Dial Professional Antibacterial and Sensitive Fragrance Free .13 g/100mL 54340-0309-02 Henkel 8 bottles — — FDA listed —
GP enMotion Antimicrobial Foam .13 g/100mL 54622-0312-01 Georgia-Pacific 1200 ml — — FDA listed —
Zep FS Antimicrobial Hand Cleaner .13 g/100mL 66949-0105-01 Zep 11400 ml — — FDA listed —
Lucky Super Soft Antibacterial Hand .13 g/100mL 76176-0024-01 NINGBO 333 ml — — Discontinued —
Hand Sanitizer .13 g/100mL 76370-0006-05 Tazza 1000 ml — — Discontinued —
Hillyard E2 Food Industry Foaming .13 g/100mL 76402-0419-02 Hillyard 1000 ml — — FDA listed —
AgroBac Pure FOAM .13 g/100mL 11084-0024-12 SC 1200 ml — — FDA listed —
Antibacterial Handwash Peach Dream .13 g/100mL 52000-0041-01 Universal 400 ml — — FDA listed —
Dial Antibacterial Frosted Cranberry and Pine .13 g/100mL 54340-0002-02 Henkel 12 bottles — — FDA listed —
GP PBU Antimicrobial Foam .13 g/100mL 54622-0313-01 Georgia 1200 ml — — FDA listed —
Zep Fuzion Antimicrobial Hand Cleaner .13 g/100mL 66949-0106-16 Zep 4800 ml — — FDA listed —
Zep Handstand Antimicrobial .13 g/100mL 66949-0127-01 Zep 9600 ml — — FDA listed —
Armor Antibacterial Body Treatment Benzalkonium Chloride .13 g/100mL 83004-0028-01 Rida 473 ml — — FDA listed —
NOxyDERM .13 g/100mL 83823-0001-01 NOxy 100 ml — — FDA listed —
Tork Hand Sanitizer Alcohol Free Foam .13 g/100mL 49351-0103-01 Essity 6 bottles — — FDA listed —
Cleanse .13 g/100mL 53329-0184-08 Medline 221 ml — — FDA listed —
Dial Antibacterial Hydrating Coconut Milk .13 g/100mL 54340-0000-02 Henkel 12 bottles — — FDA listed —
Dial Foaming Antibacterial Defense Hand Wash Linen and Lily .13 g/100mL 54340-0007-02 Henkel 6 bottles — — FDA listed —
Dial Antibacterial Peppermint Cookie Limited Seasonal .13 g/100mL 54340-0009-02 Henkel 12 bottles — — FDA listed —
Dial Antibacterial Defense Eucalyptus Mint .13 g/100mL 54340-0134-01 Henkel 12 bottles — — FDA listed —
Dial Antibacterial Defense Pomegranate and Tangerine .13 g/100mL 54340-0177-01 Henkel 325 ml — — FDA listed —
Dial Antibacterial and Sensitive Aloe .13 g/100mL 54340-0182-01 Henkel 325 ml — — FDA listed —
Dial Foaming Antibacterial Defense Coconut Water .13 g/100mL 54340-0184-01 Henkel 221 ml — — FDA listed —
Dial Foaming Antibacterial Defense Fresh Lavender .13 g/100mL 54340-0189-01 Henkel 221 ml — — FDA listed —
Zep Tranq Mdw AB Foam .13 g/100mL 66949-0387-04 Zep 6000 ml — — FDA listed —
Blue Green Foam .13 g/100mL 70411-0100-07 H2Ocean, 207 ml — — FDA listed —
Citrus Fresh Foaming Antimicrobial .13 g/100mL 76402-0420-02 Hillyard 3 bottles — — FDA listed —
Clean Choice Foodservice Antibacterial Foam .13 g/100mL 11084-0025-27 SC 1000 ml — — FDA listed —
Dial Antibacterial Hydrating Chamomile .13 g/100mL 54340-0010-02 Henkel 12 bottles — — FDA listed —
Dial Antibacterial Spring Garden Limited Seasonal .13 g/100mL 54340-0014-02 Henkel 12 bottles — — FDA listed —
Dial Foaming Antibacterial and Moisturizing Hand Wash Spring Water .13 g/100mL 54340-0016-03 Henkel 4 bottles — — FDA listed —
enMotion Antimicrobial Foam with Moisturizers Fragrance Free .13 g/100mL 54622-0314-01 Georgia-Pacific 2 bottles — — FDA listed —
enMotion Antimicrobial Foam with Moisturizers Tranquil Aloe .13 g/100mL 54622-0315-01 Georgia-Pacific 2 bottles — — FDA listed —
Zep Antibacterial HS .13 g/100mL 66949-0110-16 Zep 6000 ml — — FDA listed —
Zep Mild Antibacterial .13 g/100mL 66949-0113-24 Zep 15140 ml — — FDA listed —
Zep Blue Sky AB .13 g/100mL 66949-0124-11 Zep 6000 ml — — FDA listed —
Zoono Wound Cleanser .13 g/100mL 69221-0204-01 Zoono 50 ml — — FDA listed —
Global Care Gold Antibacterial Hand .13 g/100mL 76176-0169-01 NINGBO 400 ml — — FDA listed —
Citrus Fresh Liquid Antimicrobial .13 g/100mL 76402-0421-02 Hillyard 3 bottles — — FDA listed —
Altra Antimicrobial Foaming Hand Wash w/ Benzalkonium Chloride .13 g/100mL 30805-0018-09 Buckeye 1000 ml — — FDA listed —
ANTIBACTERIAL HANDWASH CUCUMBER and TEA TREE .13 g/100mL 52000-0048-01 Universal 400 ml — — FDA listed —
Dial Antibacterial and Sensitive Fragrance Free .13 g/100mL 54340-0174-01 Henkel 325 ml — — FDA listed —
Dial Antibacterial Defense White Tea .13 g/100mL 54340-0176-01 Henkel 325 ml — — FDA listed —
Dial Antibacterial Defense Lemon and Sage .13 g/100mL 54340-0181-01 Henkel 325 ml — — FDA listed —
Dial Foaming Antibacterial Defense Power Berries .13 g/100mL 54340-0191-01 Henkel 221 ml — — FDA listed —
Pacific Blue ultra Antimicrobial Foam Pacific Citrus .13 g/100mL 54622-0317-01 Georgia-Pacific 4 bottles — — FDA listed —
DermaCen Non-Alcohol Foaming Hand Sanitizer .13 g/100mL 62654-0141-14 Central 532 ml — — FDA listed —
Fuzion AB Foam .13 g/100mL 66949-0111-16 Zep 4800 ml — — FDA listed —
Zep FS Antimicrobial Foaming Hand Cleaner .13 g/100mL 66949-0116-16 Zep 10000 ml — — FDA listed —
Antibacterial Handwash Tropical Beach .13 g/100mL 52000-0043-01 Universal 400 ml — — FDA listed —
Dial Antibacterial Tropic Spritz Limited Seasonal .13 g/100mL 54340-0013-02 Henkel 12 bottles — — FDA listed —
Dial Antibacterial Defense Peach Citrus Punch Scent .13 g/100mL 54340-0132-01 Henkel 12 bottles — — FDA listed —
Dial Professional Antibacterial Defense Gold .13 g/100mL 54340-0302-02 Henkel 12 bottles — — FDA listed —
Pacific Blue ultra Antimicrobial Foam Fragrance Free .13 g/100mL 54622-0316-01 Georgia-Pacific 4 bottles — — FDA listed —
Zep Mango AB .13 g/100mL 66949-0128-01 Zep 3300 ml — — FDA listed —
Global Care Gold Antibacterial Hand .13 g/100mL 72146-0100-01 GLOBAL 400 ml — — FDA listed —
Antibacterial Handwash Lavender Bouquet .13 g/100mL 76176-0042-01 Ningbo 400 ml — — FDA listed —
Antibacterial Handwash Berry Medley .13 g/100mL 76176-0044-01 Ningbo 400 ml — — FDA listed —
Antibacterial Handwash Tropical Beach .13 g/100mL 76176-0043-01 Ningbo 400 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

🏛️
2020
On the market since
Jun 2020
📍
2026
Currently FDA-listed
6 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 506T60A25R
    Sorbitol is a natural sugar alcohol derived from glucose. It serves as a sweetener, humectant, and bulking agent in medications to improve taste and help maintain moisture in the product.
  • 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.

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

The official label also statesWater, Sorbitol, Fragrance

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

LabelerBLUE SEA AEROSOL & DAILY CARE CO., LTD
FDA applicationM005 (OTC MONOGRAPH DRUG)
Labeler code72119
First marketedJun 2020
Product typeHuman Otc Drug
Portfolio3 products on file

More NDCs from BLUE SEA AEROSOL & DAILY CARE CO., LTD labeler code 72119

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 📦 Storage and Handling 🧪 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 4 words ▾

Use For Hand Sanitizing

⏱️ Dosage and Administration 25 words ▾

Directions Wet hands thoroughly with product and rub until dry without wiping For children under 6, use only under adult supervision Not recommended for infants

⚠️ Warnings 7 words ▾

Warnings For external use only - Hands

📦 Storage and Handling 17 words ▾

Other information Do not store above 105F May discolor some fabrics Harmful to wood finishes and plastics

🧪 Active Ingredient 5 words ▾

Active Ingredient(s) Benzalkonium Chloride 0.13%

🧪 Inactive Ingredients 5 words ▾

Inactive ingredients Water, Sorbitol, Fragrance

🎯 Purpose 2 words ▾

Purpose Antiseptic

📄 When Using This Product 28 words ▾

When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin Do not inhale or ingest

📄 Stop Use and Ask a Doctor If 10 words ▾

Stop use and ask a doctor if skin irritation develops

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. If swallowed, get medical help or call a Poison Control Center right away.

📄 Package Label / Principal Display Panel 2 words ▾

image description

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 U HAND SANITIZER CLASSIC (this brand).

Top reported reactions

Drug Hypersensitivity118
Condition Aggravated114
Arthralgia112
Musculoskeletal Stiffness111
Pain In Extremity111
Infection110
Hepatotoxicity108

Age at onset

Infant1
Adolescent3
Adult36
Elderly10

Reporter sex

331 reports
Male · 28%
Female · 72%
Unknown · 0%

Serious outcomes

Hospitalization175
Life-threatening27
Death25
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 77 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

About this NDC listing & data coverage

Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by BLUE SEA AEROSOL & DAILY CARE CO., LTD. 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 200 ml (72119-0004-02), 473 ml (72119-0004-03). 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?
BLUE SEA AEROSOL & DAILY CARE CO., LTD 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.
← 72119-0003-01 · BLUE 72122-0001-01 · Nipro →
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.