FDA.reportPublic FDA data

75 Alcohol Hand Sanitizing Wipes

Manufacturer
E-Fresh Food Ltd.
Effective date
2021-10-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:31:57

Label at a glance#

Product75 Alcohol Hand Sanitizing Wipes
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Antibacterial (skin) cleanser. Kills harmful bacteria/germs. For personal hand hygiene to help prevent the spread of bacteria.

Dosage and administration

Adults and children over 2 years: For occasional and personal domestic use Supervise children when they use this product. Wipe hands thoroughly. Let the skin dry and discard.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • Antibacterial (skin) cleanser. Kills harmful bacteria/germs.
  • For personal hand hygiene to help prevent the spread of bacteria.

Warnings

WARNINGS SECTION

For external use only.

When using this product,

OTC - WHEN USING SECTION

avoid contact with eyes, If contact occurs, rinse thoroughly with water.

Stop use and ask / consult a doctor/ health care practitioner/health care provider / health care professional

OTC - STOP USE SECTION

if irritation develops.

KEEP OUT OF REACH OF CHILDREN.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, call a poison control center or get medical help right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 2 years:
For occasional and personal domestic use Supervise children when they use this product. Wipe hands thoroughly. Let the skin dry and discard.

Other Information

SPL UNCLASSIFIED SECTION

Keep away from open flame and sources of heat.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe barbadensis leaf extract, Water.

Questions?

OTC - QUESTIONS SECTION

Or report a serious adverse event,
Please call xxxxxxxxxxx (USA) XXXXXXXXX(CA)

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

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
80199-00880199-008-01, 80199-008-02

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
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
cea488f7-8040-8668-e053-2a95a90ad3fcad66bad7-d3a8-0c8d-e053-2a95a90ab2f42021-10-18WarningsExact identifier
spl id: cea488f7-8040-8668-e053-2a95a90ad3fc
spl set id: ad66bad7-d3a8-0c8d-e053-2a95a90ab2f4

Reported adverse events (FAERS/openFDA)#

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