FDA.reportPublic FDA data

Alcohol Wipes

Manufacturer
Kangna (Zhejiang) Medical Supplies Co., Ltd.
Effective date
2022-01-14
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:16:46

Label at a glance#

ProductAlcohol Wipes
Active ingredientALCOHOL
Label structure6 sections

Dosage and administration

●Remove lid and discard seal from container. ●Pull wipe from center of roll and thread through opening in lid. Do not push finger through opening. ●Replace lid, pull wipe up, and then out at a 45° angle. The next wipe dispenses automatically. ●Close lid to retain moisture.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

USE

INDICATIONS & USAGE SECTION

●For hand sanitizing to decrease bacteria on the skin.
●Apply topically to the skin to help prevent cross contamination.
●Not recommended for repeated use.
●Dries in seconds.

Warning

WARNINGS SECTION

●Flammable, Keep away from fire or flame. For
external use only.
●Do not use in or contact the eyes.
●Stop use and ask a doctor if too much skin irritation or
sensitivity develops or increases.

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

●Remove lid and discard seal from container.
●Pull wipe from center of roll and thread through opening in lid.
Do not push finger through opening.
●Replace lid, pull wipe up, and then out at a 45° angle. The next
wipe dispenses automatically.
●Close lid to retain moisture.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1111

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75109-50375109-503-01, 75109-503-02, 75109-503-03, 75109-503-04, 75109-503-05, 75109-503-06, 75109-503-07, 75109-503-08, 75109-503-09, 75109-503-10, 75109-503-11, 75109-503-12, 75109-503-13, 75109-503-14, 75109-503-15, 75109-503-16, 75109-503-17, 75109-503-18, 75109-503-19, 75109-503-20, 75109-503-21, 75109-503-22, 75109-503-23, 75109-503-24, 75109-503-25, 75109-503-26

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
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
d5870da1-3870-3527-e053-2995a90a7e6da88e7d0b-24f9-127d-e053-2a95a90a119f2022-01-14WarningsExact identifier
spl id: d5870da1-3870-3527-e053-2995a90a7e6d
spl set id: a88e7d0b-24f9-127d-e053-2a95a90a119f

Reported adverse events (FAERS/openFDA)#

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