FDA.reportPublic FDA data

Alcohol Wipe

Manufacturer
YAHON ENTERPRISE CO.,LTD
Effective date
2022-12-21
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:43:27

Label at a glance#

ProductAlcohol Wipe
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Open cap, remove seal and pull wipes out. Discard after single use and do not flush Keep cap and seal tightly closed between uses to prevent from drying out.

Storage and handling

Do not apply internally. Store in a cool dry place below 30˚C

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% (alc/vol)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Sanitizing wipes to help reduce bacteria on the skin or surfaces

Warnings

WARNINGS SECTION

Flammable, keep away from heat, spark, electrical fire or flame.

OTC - WHEN USING SECTION

Avoid contact with eyes. If in eyes, remove contact lenses (if any), rinse slowly with water or get medical help.

OTC - STOP USE SECTION

Stop use and ask a doctor if you have deep or puncture wounds, animal bites serious burns

Irritation and redness develop or condition persists for 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

Open cap, remove seal and pull wipes out.

Discard after single use and do not flush

Keep cap and seal tightly closed between uses to prevent from drying out.

Other information

STORAGE AND HANDLING SECTION

Do not apply internally. Store in a cool dry place below 30˚C

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Benzalkonium Chloride, Polyaminopropyl Biguanide, Citric Acid

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front LabelFront LabelBck Label Drug FactsBck Label Drug FactsWhole PackageWhole Package

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
79618-00179618-001-06

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
CITRIC ACID ACETATEDSO12WL7AUIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
POLYAMINOPROPYL BIGUANIDEDT9D8Z79ETIACT

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
236fc6c2-5257-835a-e063-6394a90a6928aafc17c6-a713-1476-e053-2a95a90a0f692024-10-01WarningsExact identifier
spl set id: aafc17c6-a713-1476-e053-2a95a90a0f69

Reported adverse events (FAERS/openFDA)#

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