Home › NDC Lookup › Ingredients › Benzalkonium Chloride › 76176-0044-01
ANTIBACTERIAL HANDWASH BERRY MEDLEY benzalkonium chloride .13 g/100mL Liquid, 400 mL — NDC 76176-0044-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

ANTIBACTERIAL HANDWASH BERRY MEDLEY benzalkonium chloride .13 g/100mL Liquid, 400 mL — NDC 76176-044-01 (Billing 76176-0044-01)

by Ningbo Liyuan Daily Chemical Products Co., Ltd. · 400 mL in 1 BOTTLE

This is a package of 400 mL of ANTIBACTERIAL HANDWASH BERRY MEDLEY benzalkonium chloride .13 g/100mL Liquid from Ningbo Liyuan Daily Chemical Products Co., Ltd., marketed since Aug 2018 and currently FDA-listed. It is this product's only package size.

NDC 76176-0044-01
🏷️ FDA NDC (as labeled) 76176-044-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 1, 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

⚠️
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) 76176-044-01
Product NDC 76176-044
11-digit billing NDC 76176004401
Application # 505G(a)(3)
SPL Set ID 751b96ae-5692-2c34-e053-2991aa0a0dfa
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2018-08-01
Route TOPICAL
Dosage form LIQUID
Substance BENZALKONIUM CHLORIDE
Why two NDCs? The FDA registers this code as 76176-044-01 — 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 → 76176-0044-01. 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.

Clinical

🧪 What is this product?

This is an over-the-counter antibacterial liquid handwash marketed under FDA's monograph rules for antiseptic skin cleansers. It contains benzalkonium chloride, a quaternary ammonium compound typically used as an antimicrobial agent in topical products to reduce bacteria on the skin. The product is intended for routine hand hygiene and is applied by washing hands with water.

Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer mLPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
76176-0044-01 You're viewing this Main listing 400 mL in 1 BOTTLE 2018-08-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
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 —
Zoono Alcohol Free Hand Sanitizer .13 g/100mL 69221-0601-11 Zoono 50 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 —
Zoono Hand Sanitizer .13 g/100mL 69221-0203-11 Zoono 50 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 —
Soft Care Instant Hand Sanitizer AF .13 g/100mL 64536-3628-03 Diversey, 1300 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 —
Purifi Hand Sanitizer .13 g/100mL 80659-0301-01 Purifi 250 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 —
U Hand Sanitizer Classic .13 g/100mL 72119-0004-01 BLUE 100 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 —
safeHands Hand Sanitizer Clean Linen .13 g/100mL 60867-0152-02 Safehands 52 ml — — 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 —
United Airlines .13 g/100mL 52305-0601-25 Freshorize 250 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 —
safeHands Hand Sanitizer Fragrance Free .13 g/100mL 60867-0150-02 Safehands 52 ml — — 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 —
Alaska Airlines .13 g/100mL 52305-0602-30 Freshorize 250 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/100mLthis 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

🏛️
2018
On the market since
Aug 2018
📍
2026
Currently FDA-listed
8 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 79G1T427CF
    A foaming and cleansing agent derived from coconut oil. It's used in topical products as a thickener and to help create lather or improve how the formula spreads on skin.
  • UNII 5OCF3O11KX
    A plant-derived surfactant made from coconut oil. It helps mix oil and water ingredients together in the formulation and can improve how the medicine spreads or feels on the skin.
  • UNII 9DBA0SBB0L
    A synthetic red dye derived from coal tar used as a colorant in medicines and cosmetics. It gives tablets, capsules, and liquids their red or pink appearance for identification and visual appeal.
  • UNII H3R47K3TBD
    FD&C Blue No. 1 is a synthetic blue dye approved for use in foods and medicines. It serves as a colorant to give the medication its distinctive appearance and help with product identification.
  • 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 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
  • UNII BPV390UAP0
    Sodium laureth sulfate is a mild detergent and surfactant derived from coconut oil or petroleum. It helps mix oil and water in formulations and is often used as a cleaning or foaming agent in topical products like shampoos and cleansers.
  • 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), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Cocamide Methyl MEA, Citric Acid, Methylisothiazolinone, lodopropynyl Butylcarbamate, Fragrance, Sodium Chloride, D&C Red No.33, FD&C Blue No.1.

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

LabelerNingbo Liyuan Daily Chemical Products Co., Ltd.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code76176
First marketedAug 2018
Product typeHuman Otc Drug
Portfolio29 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 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 10 words ▾

USES for hand washing to decrease bacteria on the skin.

⏱️ Dosage and Administration 15 words ▾

DIRECTIONS pump into hands lather vigorously for at least 5 seconds rinse and dry thoroughly.

⚠️ Warnings 22 words ▾

WARNING For external use only.

When using this product avoid contact with eyes. In case of eye contact, flush with clean water.

🧪 Active Ingredient 5 words ▾

Active Ingredient Benzalkonium Chloride 0.13%

🧪 Inactive Ingredients 14 words ▾

Inactive Ingredients: Water（Aqua),Sodium Laureth Sulfate,Cocamidopropyl Betaine,Coconut Monoethanol Amide,Sodium Chloride,Fragrance,Citric Acid,Methylchloroisothiazolinone,Methylisothiazolinone,D&C Red No.33,FD&C Blue No.1.

🎯 Purpose 2 words ▾

Purpose Antibacterial

📄 Stop Use and Ask a Doctor If 11 words ▾

STOP USE and ask a doctor if irritation and redness develops.

📄 Keep Out of Reach of Children 18 words ▾

KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center immediately.

📄 Package Label / Principal Display Panel 1 words ▾

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 Benzalkonium chloride — the ingredient across all brands.

Top reported reactions

Drug Hypersensitivity124
Arthralgia117
Condition Aggravated115
Pain In Extremity114
Infection111
Musculoskeletal Stiffness111
Joint Swelling109

Age at onset

Infant1
Child1
Adolescent3
Adult41
Elderly17

Reporter sex

479 reports
Male · 32%
Female · 68%
Unknown · 0%

Serious outcomes

Hospitalization211
Life-threatening33
Death31
Disabling23
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 51 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 Ningbo Liyuan Daily Chemical Products Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Ningbo Liyuan Daily Chemical Products 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.
← 76176-0043-01 · Ningbo 76176-0046-01 · NINGBO →
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.