Hand Sanitizer

Manufacturer: IBG Holdings Inc.
Effective date: 2020-04-10
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 23:36:35

Label at a glance#

ProductHand Sanitizer SCENTED ANTI BACTERIAL HAND SANITIZER

Active ingredientALCOHOL

Label structure11 sections

Indications and uses

■ hand sanitizer to help reduce bacteria on the skin

Dosage and administration

■ place enough product in your palm to thoroughly cover both hands ■ rub hands together until dry ■ no rinsing required

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

■ hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame. For external use only

When using this product

OTC - WHEN USING SECTION

■ avoid getting into the eyes. ■ In case of eye contact immediately flush eyes thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ if irritation or redness develops ■ condition persists for more than 72 hours ■ redness is present

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, contact a doctor or Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

■ place enough product in your palm to thoroughly cover both hands ■ rub hands together until dry ■ no rinsing required

Other information

SPL UNCLASSIFIED SECTION

■ do not store above 105ºF ■ may discolor some fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

carbomer, deionized water, propylene glycol, sodium hydroxide

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Label

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Hand Sanitizer SCENTED ANTI BACTERIAL HAND SANITIZER
Alcohol
PROPYLENE GLYCOL
WATER
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
SODIUM HYDROXIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74038-001	74038-001-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PROPYLENE GLYCOL	6DC9Q167V3	IACT
WATER	059QF0KO0R	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
cef20021-035e-3b13-e053-2995a90a0166			a240598b-d125-59b9-e053-2995a90a6dbe	2021-10-22	Warnings	Exact identifier spl set id: a240598b-d125-59b9-e053-2995a90a6dbe

Reported adverse events (FAERS/openFDA)#

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