FDA.reportPublic FDA data

Hand Sanitizing Alcohol Wipes

Manufacturer
Xiamen Yiukin Paper Products Co.,ltd
Effective date
2021-12-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:19:46

Label at a glance#

ProductHand Sanitizing Alcohol Wipes
Active ingredientALCOHOL, BENZALKONIUM CHLORIDE
Label structure9 sections

Dosage and administration

Open lid, gently pull back resealable label, remove and use wipe as required. Reseal back after use to avoid evaporation of alcohol

Storage and handling

Store at room temperature 15-30C (59-86F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 18%. Purpose: Antiseptic

Benzalkonium chloride 0.1%. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin

Apply topically to the skin to help decrease cross contamination

Not recommended for repeated use

Dries in seconds

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

Warnings

WARNINGS SECTION

Flammable, keep away from fire or flame. For external use only.

Do not use in or contact the eyes.

Stop use and ask a doctor if too much skin irritation or sensitivity develops or increases.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Open lid, gently pull back resealable label, remove and use wipe as required.

Reseal back after use to avoid evaporation of alcohol

Other information

STORAGE AND HANDLING SECTION

Store at room temperature 15-30C (59-86F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50 PC NDC: 79288-009-01

PDPPDP

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79288-00979288-009-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
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
ddee819e-1e6c-2ebe-e053-2a95a90a66cdaba41ad7-d822-f028-e053-2a95a90a61c82022-05-01WarningsExact identifier
spl set id: aba41ad7-d822-f028-e053-2a95a90a61c8

Reported adverse events (FAERS/openFDA)#

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