Alcohol

Manufacturer: Aldi, Inc | Nice-Pak Products, LLC
Effective date: 2026-01-29
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-06-01 01:35:35

Label at a glance#

ProductAlcohol

Active ingredientALCOHOL

Label structure12 sections

Indications and uses

to decrease bacteria on the skin that could cause disease recommended for repeated use

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping for children under 6, use only under adult supervision not recommended for infants

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin that could cause disease
recommended for repeated use

Warnings

WARNINGS SECTION

For exterenal use only: hands

Flammable, keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop
condition persists for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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 without wiping
for children under 6, use only under adult supervision
not recommended for infants

Other information

SPL UNCLASSIFIED SECTION

do not store above 105⁰F
may discolor some fabrics
harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, carbomer and/or acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, glycerin, isopropyl myristate, tocopheryl acetate

SPL UNCLASSIFIED SECTION

*Effective at eliminating 99.99% of many common harmful germs and bacteria in as little as 15 seconds.

Dist. & Sold Exclusively By: ALDI

Batavia, IL 60510

ALDI TWICE AS NICE GUARANTEE

items replaced

money refunded

Empty & Discard Pump

PLASTIC BOTTLE

how2recycle.info

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LACURA ^®

Moisturizing

Hand Sanitizer

KILLS 99.99% OF GERMS*

GREEN SEAL CERTIFIED ^®

greenseal.org

8 FL. OZ (236 mL)

image description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
64024-849-16	Alcohol	59 mL in 1 BOTTLE, PLASTIC	LIQUID	59	5
64024-849-34	Alcohol	236 mL in 1 BOTTLE, PLASTIC	LIQUID	236	5
64024-849-45	Alcohol	946 mL in 1 BOTTLE, PLASTIC	LIQUID	946	5

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Alcohol
WATER
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
GLYCERIN
ISOPROPYL MYRISTATE
TOCOPHEROL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
64024-849	64024-849-16, 64024-849-45, 64024-849-34

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	IACT
GLYCERIN	PDC6A3C0OX	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
TOCOPHEROL	R0ZB2556P8	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
Alcohol	ALCOHOL	Aldi, Inc	aaa55815-ab6d-41c0-b04f-53de8001ebc7	2026-01-29	Warnings	Exact identifier ndc (package): 64024-849-34 ndc (package): 64024-849-45 ndc (package): 64024-849-16 ndc (product): 64024-849 ndc11 (package): 64024084916 ndc11 (package): 64024084934 ndc11 (package): 64024084945 spl id: 498c60b0-32a4-b619-e063-6294a90a7d59 spl set id: aaa55815-ab6d-41c0-b04f-53de8001ebc7

Reported adverse events (FAERS/openFDA)#

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