Alcohol Wet Wipes

Manufacturer
Wenzhou Guanshang Paper Co., Ltd | A03 Lab of BTS
Effective date
2020-07-22
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:20:32

Label at a glance#

ProductAlcohol Wet Wipes
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Unfold towlette, wipe hands, discard after use.

Storage and handling

Please put it in a cool and dry place, avoid direct sunlight.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic.

When using

OTC - WHEN USING SECTION

Avoid using in eyes, wounds and other sensitive parts.

If it gets into eyes accidentally, please wash it with plenty of water.

Do not use

OTC - DO NOT USE SECTION

Do not use in eyes, wounds and other sensitive parts.

Stop use

OTC - STOP USE SECTION

Stop use if irritation and redness develop. If condition continues, consult your health care practitioner.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Do not let children touch it.

Indications & usage

INDICATIONS & USAGE SECTION

Sterilization, killing intestinal carcinogenic bacteria, laboratory cocci, pathogenic yeast and common bacteria of hospital infection.

This product is suitable for wiping hands, face, skin, etc.

Directions

DOSAGE & ADMINISTRATION SECTION

Unfold towlette, wipe hands, discard after use.

Warnings

WARNINGS SECTION

For external use only.

Flammable, please stay away from fire or heat.

Other information

STORAGE AND HANDLING SECTION

Please put it in a cool and dry place, avoid direct sunlight.

Inactive ingredient

INACTIVE INGREDIENT SECTION

Water.

Package label. Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Blue50Blue50

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78122-10278122-102-15, 78122-102-21, 78122-102-25, 78122-102-13

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
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
eebc8eb3-54b2-491d-e053-2a95a90a0f98a6f19840-63b6-9448-e053-2a95a90af1202022-11-30WarningsExact identifier
spl set id: a6f19840-63b6-9448-e053-2a95a90af120

Reported adverse events (FAERS/openFDA)#

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