FDA.reportPublic FDA data

Alcohol Wipes

Manufacturer
WellBe Si International Co., Ltd.
Effective date
2021-01-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:57:52

Label at a glance#

ProductAlcohol Wipes
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Rub wipe over all surfaces of both hands and allow to dry. Supervise children under 6 years old.

Storage and handling

Please keep away from fire or direct sunlight, and keep out of reach of children.

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.

Recommend for repeated use.

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

When using this product keep away from the eyes. In case of eye contact, rinse eyes with water.

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

Keep out of reach of children. If swallowed get medical help or contact a poison control center immediately.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop for 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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Rub wipe over all surfaces of both hands and allow to dry. Supervise children under 6 years old.

Other information

STORAGE AND HANDLING SECTION

Please keep away from fire or direct sunlight, and keep out of reach of children.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Ethanol, Benzethonium Chloride, Zinc Pyrithione, Ethylhexylglycerin, 2-phenoxyethanol, Aloe Barbadensis Leaf Juice, Water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front and Back LabelsFront and Back Labels

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81384-00181384-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ETHYLHEXYLGLYCERIN147D247K3PIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
PHENOXYETHANOLHIE492ZZ3TIACT
BENZETHONIUM CHLORIDEPH41D05744IACT
PYRITHIONE ZINCR953O2RHZ5IACT
ALOE VERA LEAFZY81Z83H0XIACT

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
e8210560-7042-4b26-e053-2995a90ae3d5b832d7c2-38e0-82b6-e053-2a95a90a363b2022-09-07WarningsExact identifier
spl set id: b832d7c2-38e0-82b6-e053-2a95a90a363b

Reported adverse events (FAERS/openFDA)#

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