FDA.reportPublic FDA data

HAND SANITIZER WIPES

Manufacturer
Zhejiang Qimei Cosmetics Co., Ltd.
Effective date
2021-04-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:45:42

Label at a glance#

ProductHAND SANITIZER WIPES
Active ingredientALCOHOL
Label structure15 sections

Indications and uses

to decrease bacteria on the skin that could cause disease

Dosage and administration

wet hands thoroughly with product and allow to dry not recommended for infants

Storage and handling

do not store above 105ºF may discolor some fabrics harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin that could cause disease

Warnings

WARNINGS SECTION

For external use only: hands

Flammable. Keep away from fire and flame.

OTC - WHEN USING SECTION

When using this product

keep out of eyes. In case of contact with eyes, flush thoroughly with water.
avoid contact with broken skin
do not inhale or ingest

OTC - STOP USE SECTION

Stop use and ask a doctor if

irritation or redness develops
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

wet hands thoroughly with product and allow to dry

not recommended for infants

other information

STORAGE AND HANDLING SECTION

do not store above 105ºF
may discolor some fabrics
harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe barbadensis leaf juice, glycerin, isopropanol, propanediol, tocopheryl acetate, water

Uses

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin that could cause disease

recommended for repeated use

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product and allow to dry without wiping
not recommended for infants

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

20 WIPES, NDC: 81773-001-01

20 WIPES Label20 WIPES Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

160 WIPES, NDC: 81773-001-03

160 WIPES Label160 WIPES Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50 WIPES, NDC: 81773-001-02

50 WIPES Label50 WIPES Label

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81773-00181773-001-01, 81773-001-02, 81773-001-03

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
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
PROPANEDIOL5965N8W85TIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ISOPROPYL ALCOHOLND2M416302IACT

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
bfe55d1c-4934-653e-e053-2a95a90adee3bfe55d1c-4933-653e-e053-2a95a90adee32021-04-28WarningsExact identifier
spl id: bfe55d1c-4934-653e-e053-2a95a90adee3
spl set id: bfe55d1c-4933-653e-e053-2a95a90adee3

Reported adverse events (FAERS/openFDA)#

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