FDA.reportPublic FDA data

Hand Sanitizing Wipes

Manufacturer
INOVAGEL MÉXICO, S.A. DE C.V.
Effective date
2024-01-17
Label type
HUMAN OTC DRUG LABEL
Version
12
Source
legacy-cache
Hydrated at
2026-08-01 21:14:05

Label at a glance#

ProductHand Sanitizing Wipes
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Adults and children 6 years and older: Rub wipe thoroughly over all surfaces of hands and allow to dry Children under 6 years: Should be supervised when using this product

Storage and handling

To dispose: Place in wastebasket after use. Do not flush

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70%. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

To help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable until dry. Keep away from heat or flame

For external use only.

OTC - WHEN USING SECTION

When using this product

  • Do not use in or near the eyes.
  • In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs.

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.

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 6 years and older: Rub wipe thoroughly over all surfaces of hands and allow to dry
  • Children under 6 years: Should be supervised when using this product

Other information

STORAGE AND HANDLING SECTION

  • To dispose: Place in wastebasket after use.
  • Do not flush

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Water.

Package container Hand Sanitizing Wipes, 70% alcohol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ALC_BOTEALC_BOTENDC: 81575-001-05 Container

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
81575-00181575-001-05

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
GLYCERINPDC6A3C0OXIACT
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
2a33d462-6d0e-7d92-e063-6294a90a5c86bde7aeda-b485-26ef-e053-2a95a90accb12024-12-26WarningsExact identifier
spl set id: bde7aeda-b485-26ef-e053-2a95a90accb1

Reported adverse events (FAERS/openFDA)#

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