FDA.reportPublic FDA data

Benzalkonium Chloride

Manufacturer
ALO NEW YORK LLC
Effective date
2026-01-15
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:33:23

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 fron 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 ingredients

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 - WHEN USING SECTION

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

Keep out of the 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 fron 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

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Decyl Glucoside, Aloe Barbadensis (Aloe) Leaf Extract, Phenoxyethanol, Citric Acid, Sodium Benzoate, Potassium Sorbate, Eucalyptus Globulus Oil, Mentha Piperita (Peppermint) Oil.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ALO

20 Skin-Softening Sanitizing Hand Wipes

20 Count Wipes20 Count Wipes

ALO

20 Individually Wrapped Sanitizing Hand Wipes

20 Individually Wrapped Wipes20 Individually Wrapped Wipes

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN6
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD6
1038558benzalkonium chloride 0.13 % Topical ClothSY6
1038558benzalkonium chloride 0.13 % Topical SwabSY6
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY6
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY6
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82355-550-01Benzalkonium Chloride1 mg in 1 PACKAGECLOTH16
82355-550-01Benzalkonium Chloride20 in 1 PACKAGECLOTH206
82355-550-02Benzalkonium Chloride1 mg in 1 PACKAGECLOTH16
82355-550-02Benzalkonium Chloride20 in 1 PACKAGECLOTH206

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82355-55082355-550-02, 82355-550-01

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
NameUNIIKind
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
MENTHA PIPERITA79M2M2UDA9IACT
SODIUM BENZOATEOJ245FE5EUIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
DECYL GLUCOSIDEZ17H97EA6YIACT
EUCALYPTUS GLOBULUS WHOLESI1P2XF3M3IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
POTASSIUM SORBATE1VPU26JZZ4IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52025-12-05monthly-update2026-06-03 17:45:26

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 ChlorideSANITIZING HAND WIPESALO NEW YORK LLCd3afde78-b9f6-3648-e053-2a95a90a40242026-01-15WarningsExact identifier
ndc (package): 82355-550-02
ndc (package): 82355-550-01
ndc (product): 82355-550
ndc11 (package): 82355055001
ndc11 (package): 82355055002
spl id: 48751555-8dc5-33e6-e063-6394a90aec65
spl set id: d3afde78-b9f6-3648-e053-2a95a90a4024

Reported adverse events (FAERS/openFDA)#

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