FDA.reportPublic FDA data

ANTIBACTERIAL HANDWASH

Manufacturer
Click Products LLC
Effective date
2020-10-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:32:30

Label at a glance#

ProductANTIBACTERIAL HANDWASH HOBBY
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

For Handwashing to decrease bacteria on the skin

Dosage and administration

Pump into hands ,wet as needed lather vigorously for at least 15 seconds Wash skin, rinse throughly and dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

USES

INDICATIONS & USAGE SECTION

  • For Handwashing to decrease bacteria on the skin

WARNING

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

  • avoid contact with eyes.
  • In case of eye contact, flush with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • If irritation and redness develops.

KEEP OUT OF REACH OF CHILDREN.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center immediately.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • Pump into hands ,wet as needed
  • lather vigorously for at least 15 seconds
  • Wash skin, rinse throughly and dry.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water（Aqua),Cocamidopropyl Betaine,Sodium Chloride,Fragrance, Citric Acid,Methylchloroisothiazolinone,Methylisothiazolinone,  Cocamide/DEA, FD&C Blue No1, FD&C Red No 40,Glycerin ,Parfum,Tetrasodium EDTA,Sodium laureth sultate.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

44

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN2
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD2
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY2
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71611-072-50ANTIBACTERIAL HANDWASHHOBBY500 mL in 1 BOTTLELIQUID5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71611-072ANTIBACTERIAL HANDWASH HOBBY (BENZALKONIUM CHLORIDE) LIQUID [CLICK PRODUCTS LLC]2Legacy NDC, 1 package rows20201028_9ea8142a-d020-423c-afde-3b548365e8b5.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71611-07271611-072-50

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
SODIUM CHLORIDE451W47IQ8XIACT
WATER059QF0KO0RIACT
SODIUM LAURETH-3 SULFATEBPV390UAP0IACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
COCO DIETHANOLAMIDE92005F972DIACT
DMDM HYDANTOINBYR0546TOWIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
GLYCERINPDC6A3C0OXIACT
EDETATE SODIUMMP1J8420LUIACT
SULISOBENZONE1W6L629B4KIACT
FD&C RED NO. 40WZB9127XOAIACT
BENZYL ALCOHOLLKG8494WBHIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
b2a9efc0-d3ef-48be-e053-2a95a90a2f009ea8142a-d020-423c-afde-3b548365e8b52020-10-27WarningsExact identifier
spl id: b2a9efc0-d3ef-48be-e053-2a95a90a2f00
spl set id: 9ea8142a-d020-423c-afde-3b548365e8b5

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.