ALCOHOL WIPES

Manufacturer
Henan Meishiyu Sanitary Products Co., Ltd | A03 Lab of BTS
Effective date
2020-07-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:21:43

Label at a glance#

ProductALCOHOL WIPES
Active ingredientBENZALKONIUM CHLORIDE, ALCOHOL
Label structure12 sections

Dosage and administration

Uncover the seal on the package, take out the Wipes and directly wipe the object and skin surface directly.

Storage and handling

Please close the cover and keep it sealed after use. Alcohol by nature evaporates quickly. This product is insoluble in water. Please do not put it into the toilet after use.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol 12% v/v, Benzalkonium chloride 0.005% v/v

Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

When Using

OTC - WHEN USING SECTION

When using this product keep out of eyes.

In case of contact with eyes, rinse eyes throughly with water.

Do not use

OTC - DO NOT USE SECTION

in or contact the eyes

Stop use

OTC - STOP USE SECTION

Discontinue if irritation and redness develop. If the condition persists for more than 72 hours, consult a physician.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Indications & usage

INDICATIONS & USAGE SECTION

It has bactericidal effect on Escherichia coli, Staphylococcus aureus and Candida albicans.

These wipes are meant for general cleansing.

Cleaning and disinfection of object surfaces, especially hands and skin.

Directions

DOSAGE & ADMINISTRATION SECTION

Uncover the seal on the package, take out the Wipes and directly wipe the object and skin surface directly.

Warnings

WARNINGS SECTION

For external use only.

These wipes do not replace wipes used for medical procedures.

Flammable. Keep in a dry place away from fire.

Other information

STORAGE AND HANDLING SECTION

Please close the cover and keep it sealed after use. Alcohol by nature evaporates quickly.

This product is insoluble in water. Please do not put it into the toilet after use.

Inactive ingredient

INACTIVE INGREDIENT SECTION

Water

Package label. Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1010

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78922-10178922-101-05, 78922-101-13, 78922-101-19

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
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
f55884ec-3c56-0e8c-e053-2995a90ae93aa8251629-598c-1866-e053-2a95a90af3422023-02-23WarningsExact identifier
spl set id: a8251629-598c-1866-e053-2a95a90af342

Reported adverse events (FAERS/openFDA)#

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