Hand Sanitizer

Manufacturer: Medline Industries, LP
Effective date: 2026-02-11
Label type: HUMAN OTC DRUG LABEL
Version: 14
Source: full-release
Hydrated at: 2026-06-01 01:43:55

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure9 sections

Dosage and administration

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

Contacts and useful links#

Websitewww.medline.com

www.medline.com

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only: hands only

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 or redness develops
condition persists for more than 72 hours

Keep out of reach 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 suervision
not recommended for infants

Other information

SPL UNCLASSIFIED SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, glyceryl caprylate/caprate, isopropyl myristate, meadowfoamamidopropyl betaine, PEG-8 dimethicone, tocopheryl acetate, water

Manufacturing Information

SPL UNCLASSIFIED SECTION

Manufactured for:

Medline Industries, LP

Three Lakes Drive, Northfield, IL 60093 USA

Made in USA with US and foreign components

www.medline.com

1-800-MEDLINE

REF: HH701200F

V2 RB23VJO

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front Label V2 RB23VJO

Back Label V2 RB23VJO

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
53329-209-12	Hand Sanitizer	44 mL in 1 BOTTLE, PUMP	LIQUID	44	14
53329-209-37	Hand Sanitizer	221 mL in 1 BOTTLE, PUMP	LIQUID	221	14
53329-209-74	Hand Sanitizer	1200 mL in 1 BOTTLE	LIQUID	1200	14
53329-209-80	Hand Sanitizer	532 mL in 1 BOTTLE, PUMP	LIQUID	532	14
53329-209-98	Hand Sanitizer	1000 mL in 1 BOTTLE, PUMP	LIQUID	1000	14

Products#

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

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

Hand Sanitizer
Alcohol
PEG-8 DIMETHICONE
MEADOWFOAMAMIDOPROPYL BETAINE
WATER
GLYCERYL CAPRYLATE/CAPRATE
GLYCERIN
.ALPHA.-TOCOPHEROL ACETATE
ISOPROPYL MYRISTATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
53329-209	53329-209-98, 53329-209-80, 53329-209-37, 53329-209-74, 53329-209-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PEG-8 DIMETHICONE	GIA7T764OD	IACT
MEADOWFOAMAMIDOPROPYL BETAINE	HNV0L650LG	IACT
WATER	059QF0KO0R	IACT
GLYCERYL CAPRYLATE/CAPRATE	G7515SW10N	IACT
GLYCERIN	PDC6A3C0OX	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	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
Hand Sanitizer	ALCOHOL	Medline Industries, LP	42813b3e-dfae-495c-bffb-bf3862857cb1	2026-02-11	Warnings	Exact identifier ndc (package): 53329-209-12 ndc (package): 53329-209-74 ndc (package): 53329-209-80 ndc (package): 53329-209-37 ndc (package): 53329-209-98 ndc (product): 53329-209 ndc11 (package): 53329020980 ndc11 (package): 53329020937 ndc11 (package): 53329020974 ndc11 (package): 53329020912 ndc11 (package): 53329020998 spl id: 4a8e3274-7e1a-8509-e063-6394a90a8149 spl set id: 42813b3e-dfae-495c-bffb-bf3862857cb1

Reported adverse events (FAERS/openFDA)#

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