FDA.reportPublic FDA data

HAND SANITIZING WIPES

Manufacturer
Dalian Daxin Nonwoven Technology Co., Ltd.
Effective date
2022-01-14
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:16:45

Label at a glance#

ProductHAND SANITIZING WIPES
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Dosage and administration

Directions● Adults and children 2 yrs and over, apply to hands and allow skin to dry without wiping. ●Children under 2, ask doctor before use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.3%

Purpose

OTC - PURPOSE SECTION

Antibacterial

USE

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.
Recommended for repeated use.

Warning

WARNINGS SECTION

For external use only. Do not use if you are allergic to
any of the ingredients.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions● Adults and children 2 yrs and over,
apply to hands and allow skin to dry without wiping.
●Children under 2, ask doctor before use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Phenoxyethanol, Sodium
benzoate, Propylene glycol, Aloe barbadensis leaf juice, PEG-8
dimethicone, Benzethonium chloride, Disodium edta, Citric acid.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

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
78028-00178028-001-01

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
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
PROPYLENE GLYCOL6DC9Q167V3IACT
PEG-8 DIMETHICONEGIA7T764ODIACT
ALOE VERA LEAFZY81Z83H0XIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
BENZETHONIUM CHLORIDEPH41D05744IACT
DISODIUM EDTA-COPPER6V475AX06UIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SODIUM BENZOATEOJ245FE5EUIACT

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
d5983300-ccab-b9c9-e053-2a95a90a471da61df630-e883-6b07-e053-2995a90ab9122022-01-14WarningsExact identifier
spl id: d5983300-ccab-b9c9-e053-2a95a90a471d
spl set id: a61df630-e883-6b07-e053-2995a90ab912

Reported adverse events (FAERS/openFDA)#

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