Hand Sanitizer

Manufacturer: Shandong Aoyou Biotechnology Co.,Ltd
Effective date: 2020-05-10
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:10:38

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure10 sections

Indications and uses

to decrease bacteria on the skin that could cause disease . recommended for repeat 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 recommend for infants.

Storage and handling

do not store above 105°F may discolor some fabric harmful to wood finishes and plastic.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external 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

OTC - STOP USE SECTION

Stop using and ask a doctor if irritation or redness develops.condition persists for more than 72 hours.

Keep out of reach of children.lf 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 recommend for infants.

Other Information

STORAGE AND HANDLING SECTION

do not store above 105°F

may discolor some fabric

harmful to wood finishes and plastic.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

purified water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500 ml label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75118-002-01	2021-07-23	C162847	48780-1	c7ccaba7-1ed2-fd44-e053-dadaa90aa01b	Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75118-002-01	Hand Sanitizer	500 mL in 1 BOTTLE	GEL	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75118-002	HAND SANITIZER GEL [SHANDONG AOYOU BIOTECHNOLOGY CO.,LTD]	1	Legacy NDC, 1 package rows	20200511_a548aa0e-e0c3-5ddb-e053-2995a90abe1d.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Hand Sanitizer
TRICLOSAN
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75118-002	75118-002-01

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
Name	UNII	Kind
TRICLOSAN	4NM5039Y5X	IACT
WATER	059QF0KO0R	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
a5477eb1-8b38-46ac-e053-2995a90a60d4			a548aa0e-e0c3-5ddb-e053-2995a90abe1d	2020-05-10	Warnings	Exact identifier spl id: a5477eb1-8b38-46ac-e053-2995a90a60d4 spl set id: a548aa0e-e0c3-5ddb-e053-2995a90abe1d