Label at a glance#

ProductBoardwalk

Active ingredientBENZALKONIUM CHLORIDE

Label structure11 sections

Indications and uses

For handwashing to decrease bacteria on the skin

Dosage and administration

For use apply thoroughly to hands and face as desired. Allow to dry without wiping. Discard wipe in trash receptacle after use. Do not flush. For dispensing tear open package at notch. Dispose of wrapper in trash. Do not flush

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.115%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

in the eyes
if you are allergic to any of the ingredients

When using this product

OTC - WHEN USING SECTION

If eye contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

if irritation and redness develops and persists for more than 72 hours.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed contact a doctor or Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

For use apply thoroughly to hands and face as desired. Allow to dry without wiping. Discard wipe in trash receptacle after use. Do not flush.
For dispensing tear open package at notch. Dispose of wrapper in trash. Do not flush

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Aloe Barbadensis Leaf Extract, Disodium Cocoamphodiacetate, SD Alcohol 40-B, Methylchloroisothiazolinone, Methylisothiazolinone, Tocopheryl Acetate, Disodium EDTA, Citric Acid, Fragrance

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Boardwalk AB Label

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1049374	Benzalkonium (Topical)	benzalkonium chloride 1.15 MG/ML Medicated Pad	SCD Active

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

Boardwalk
Benzalkonium Chloride
WATER
ALOE VERA LEAF
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
EDETATE DISODIUM
CITRIC ACID MONOHYDRATE
BENZALKONIUM
DISODIUM COCOAMPHODIACETATE
ALPHA-TOCOPHEROL ACETATE
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71906-055	71906-055-75

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
EDETATE DISODIUM	7FLD91C86K	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
DISODIUM COCOAMPHODIACETATE	18L9G3U51M	IACT
ALPHA-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
ALCOHOL	3K9958V90M	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ce3bc363-3fa4-9cf5-e053-2995a90a2b64			71c57d9d-7022-91cb-e053-2a95a90ab428	2021-10-13	Warnings	Exact identifier spl set id: 71c57d9d-7022-91cb-e053-2a95a90ab428

Reported adverse events (FAERS/openFDA)#

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

Boardwalk