FDA.reportPublic FDA data

ALCOHOL WIPES

Manufacturer
Henan Meishiyu Sanitary Products Co., Ltd.
Effective date
2020-09-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:15:51

Label at a glance#

ProductALCOHOL WIPES
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

to decrease bacteria on the skin recommended for repeated use

Dosage and administration

rub wipe 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

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

USES

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin

recommended for repeated use

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

rub wipe 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

WARNINGS

WARNINGS SECTION

For external use only.

Flammable, keep product away from fire or flame.

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

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

KEEP OUT OF REACH OF CHILDREN

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 immediately.

STOP USE

OTC - STOP USE SECTION

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

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Benzalkonium Chloride，water

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50 CLOTH IN I BAG NDC: 78922-002-01

Label 1Label 1Label 2Label 2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78922-002-012023-02-23C16284748780-1f386c649-9caa-0266-e053-dadaa90a7c1aALCOHOL WIPES
78922-002-012023-01-30C16284748780-1f386c649-9caa-0266-e053-dadaa90a7c1aALCOHOL WIPES

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
78922-00278922-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT

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
f5597919-ef46-c4c4-e053-2995a90a40d3aecffb63-ac35-7dd0-e053-2a95a90a1c182023-02-23WarningsExact identifier
spl set id: aecffb63-ac35-7dd0-e053-2a95a90a1c18

Reported adverse events (FAERS/openFDA)#

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