Alcohol Wipe

Manufacturer: IMEI CHEMICAL ENTERPRISE LTD.
Effective date: 2020-07-01
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:22:59

Label at a glance#

ProductAlcohol Wipe

Active ingredientALCOHOL

Label structure10 sections

Dosage and administration

Open packet, remove and unfold wipe, wipe hands thoroughly, do not flush.

Storage and handling

Do not store above 105F/40C. Store in a cool dry place, away for direct sunlight.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only, do not inhale or ingest

Flammable keep away from fireor flame or direct sunlight

OTC - WHEN USING SECTION

When using the product keep out of eyes. In case of eye contact, flush thoroughly with water and get medical help

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

For children under 6, use only under adult supervision. Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Open packet, remove and unfold wipe, wipe hands thoroughly, do not flush.

Other information

STORAGE AND HANDLING SECTION

Do not store above 105F/40C. Store in a cool dry place, away for direct sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front and Back LabelsOne Wipe, NDC: 77660-203-01

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Alcohol Wipe
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77660-203	77660-203-01

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
c70633b1-5245-03ca-e053-2995a90af861			a96cdc0f-e56d-493e-e053-2a95a90a63e8	2021-07-13	Warnings	Exact identifier spl set id: a96cdc0f-e56d-493e-e053-2a95a90a63e8

Reported adverse events (FAERS/openFDA)#

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