FDA.reportPublic FDA data

Hand Sanitizing Wipes

Manufacturer
Hangzhou Linkeweier Daily Chemicals Co. Ltd.
Effective date
2021-02-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:50:03

Label at a glance#

ProductHand Sanitizing Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Indications and uses

For handwashing to decrease bacteria on the skin. After changing diapers. After assisting ill persons. Before contact with a person under medical care or treatment. Recommended for repeat use.

Dosage and administration

Wet hands thoroughly with product and allow to dry. Children under six years of age should be supervised when using this product.

Storage and handling

Store in a cool, dry place.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.08%

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

USES

INDICATIONS & USAGE SECTION

  • For handwashing to decrease bacteria on the skin.
  • After changing diapers.
  • After assisting ill persons.
  • Before contact with a person under medical care or treatment.
  • Recommended for repeat use.

WARNING

WARNINGS SECTION

For external use only.

Do not use in the eyes.

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

When using this product do not get into eyes. If contact occurs, rinse thoroughly with water.

STOP USE AND ASK A DOCTOR IF

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach from children. If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry.
  • Children under six years of age should be supervised when using this product.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

Store in a cool, dry place.

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Decyl Glucoside，Polyaminopropyl Biguanide，Phenoxyethanol， Didecyl Dimethyl Ammonium Chloride，Aloe Barbadensis Leaf Juice Glyceri，Vitamin E, Water

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

800 IN A BAG NDC: 71766-004-01

Label-800 in bagLabel-800 in bag

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71766-00471766-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
DECYL GLUCOSIDEZ17H97EA6YIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYAMINOPROPYL BIGUANIDEDT9D8Z79ETIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT

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
bb1f9a96-4eba-6dd6-e053-2a95a90a6248bb1f9a96-4eb9-6dd6-e053-2a95a90a62482021-02-12WarningsExact identifier
spl id: bb1f9a96-4eba-6dd6-e053-2a95a90a6248
spl set id: bb1f9a96-4eb9-6dd6-e053-2a95a90a6248

Reported adverse events (FAERS/openFDA)#

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