Label at a glance#

ProductHand sanitizer

Active ingredientALCOHOL

Label structure11 sections

Indications and uses

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

Label contents#

Full prescribing information#

Uses

DOSAGE & ADMINISTRATION SECTION

to decrease bacteria on the skin that could cause disease.

recommended for repeated use.

WARNINGS SECTION

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

OTC - WHEN USING SECTION

keep out of eyes.

ln case of contact with eyes.

flush thoroughly with water.

avoid contact with broken skin .

do not inhale or ingest.

OTC - STOP USE SECTION

irritation or redness develops .

condition persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed. get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE SECTION

Place enough product on hands to cover all surfaces.Rub hands together until dry.Supervise children under 6 years of agewhen using this product to avoid swallowing.

other information

HOW SUPPLIED SECTION

Do not store above 105°F

May discolor some fabrics

Harmful to wood finishes and plastics.

INACTIVE INGREDIENT SECTION

purified water

OTC - ACTIVE INGREDIENT SECTION

ALCOHOL 75%

OTC - PURPOSE SECTION

Disinfection
Sterilization

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1305100	Ethanol (Topical)	ethanol 0.75 ML/ML Topical Gel	SCD Active

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1305100	ethanol 75 % Topical Gel	PSN	1
1305100	ethanol 0.75 ML/ML Topical Gel	SCD	1
1305100	ethanol 75 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
55469-008-01	2022-01-28	C162847	48780-1	d6a99b39-8067-a426-e053-dadaa90af4c2	b4fd6a78-983c-b692-e053-2995a90a06e0

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55469-008-01	Hand sanitizer	300 mL in 1 BOTTLE	GEL	300		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55469-008	HAND SANITIZER GEL [DONGYANG LIULU COSMETICS CO.LTD]	1	Legacy NDC, 1 package rows	20201127_b4fd6a78-983c-b692-e053-2995a90a06e0.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Hand sanitizer
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
55469-008	55469-008-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
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
b4fd6a78-983d-b692-e053-2995a90a06e0			b4fd6a78-983c-b692-e053-2995a90a06e0	2020-11-26	Warnings	Exact identifier spl id: b4fd6a78-983d-b692-e053-2995a90a06e0 spl set id: b4fd6a78-983c-b692-e053-2995a90a06e0

Reported adverse events (FAERS/openFDA)#

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

Hand sanitizer