FDA.reportPublic FDA data

Benzalkonium Chloride

Manufacturer
Target Corporation
Effective date
2025-12-05
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:20:29

Label at a glance#

ProductBenzalkonium Chloride
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

for hand sanitizing to decrease bacteria on the skin recommended for repeated use

Dosage and administration

adults and children 2 years and over: apply to hands; allow to dry without wiping. Children under 2 years: ask a doctor before use. To dispense: Peel back front label slowly. Remove wipes. To reseal: Firmly rub thumb over label. Dispose of wipe in trash. Do not flush.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • for hand sanitizing to decrease bacteria on the skin
  • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

if you are allergic to any of these ingredients.

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or redness develops, or if condition persists for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 2 years and over: apply to hands; allow to dry without wiping.
  • Children under 2 years: ask a doctor before use.
  • To dispense: Peel back front label slowly. Remove wipes.
  • To reseal: Firmly rub thumb over label. Dispose of wipe in trash. Do not flush.

Other information

OTHER SAFETY INFORMATION

  • store below 95°F (35°C)
  • keep closed tightly
  • may discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Phenoxyethanol, Decyl Glucoside, Disodium EDTA, Sodium Benzoate, Potassium Sorbate, Vitamin E, Aloe Barbadensis Leaf Extract, Citric Acid, Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

antibacterial

hand wipes

plant-based wipes

dermatologist tested

hypoallergenic

25 HAND WIPES

5½ IN X 8 IN

L1L1

40 HAND WIPES

5½ IN X 8 IN

L2L2

72 HAND WIPES

5½ IN X 8 IN

L3L3

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN4
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD4
1038558benzalkonium chloride 0.13 % Topical ClothSY4
1038558benzalkonium chloride 0.13 % Topical SwabSY4
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY4
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY4
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82442-250-25Benzalkonium Chloride25 in 1 CONTAINERCLOTH254
82442-250-40Benzalkonium Chloride40 in 1 CONTAINERCLOTH404
82442-250-72Benzalkonium Chloride72 in 1 CONTAINERCLOTH724

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82442-25082442-250-40, 82442-250-72, 82442-250-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
PHENOXYETHANOLHIE492ZZ3TIACT
WATER059QF0KO0RIACT
SODIUM BENZOATEOJ245FE5EUIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
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
Benzalkonium ChlorideANTIBACTERIAL HAND WIPESTarget Corporationf6037707-c6bb-11a0-e053-2995a90acce82025-12-05WarningsExact identifier
ndc (package): 82442-250-40
ndc (package): 82442-250-72
ndc (package): 82442-250-25
ndc (product): 82442-250
ndc11 (package): 82442025072
ndc11 (package): 82442025025
ndc11 (package): 82442025040
spl id: 453a6c6e-a1f9-e2e3-e063-6294a90ae7f4
spl set id: f6037707-c6bb-11a0-e053-2995a90acce8

Reported adverse events (FAERS/openFDA)#

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