Alcohol Wipe

Manufacturer
YAHON ENTERPRISE CO.,LTD
Effective date
2022-12-21
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:43:31

Label at a glance#

ProductAlcohol Wipe
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Rub wire thoroughly over all surfaces of both hands and allow to dry. Supervise children under 6 years old. Not recommended for infants Discard wipe in trash; do not flush

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin

Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or redness develop or last more than 72 hours

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Rub wire thoroughly over all surfaces of both hands and allow to dry.

Supervise children under 6 years old.

Not recommended for infants

Discard wipe in trash; do not flush

Inactive ingredients

INACTIVE INGREDIENT SECTION

Benzalkonium Chloride, Citric Acid, Polyaminopropyl Biguanide Water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front and Back LabelsFront and Back Labels50 wipes NDC: 79618-001-08

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
79618-00179618-001-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
236fc9b0-64da-88cd-e063-6394a90a06a8b3038abe-4d70-d97e-e053-2995a90aeee82024-10-01WarningsExact identifier
spl set id: b3038abe-4d70-d97e-e053-2995a90aeee8

Reported adverse events (FAERS/openFDA)#

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