Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.

WARNINGS SECTION

Warnings• For external use only

• Flammable, keep away from fire or flame

• Do not use in eyes. In case of contact, rinse eyes thorougly with water.

• Discontinue use if irritation and redness develop.If condition persists for more than 72 hours consult a doctor.

• Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out of Reach of Children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Aloe Barbadensis Leaf Juice, Denatonium Benzoate, Fragrance, Glycerin, Maltodextrin, Propylene Glycol, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MiniCCLabel-01

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1020364	ethanol 0.62 ML/ML Topical Spray	ethanol 0.62 ML/ML Topical Spray	SCD Active

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1020364	ethanol 62 % Topical Spray	PSN	1
1020364	ethanol 0.62 ML/ML Topical Spray	SCD	1
1020364	ethanol 62 % Topical Spray	SY	1
1020364	ethyl alcohol 62 % Topical Spray	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
65692-2052-1	2024-01-30	C162847	48780-1	1030e365-65e8-111a-e063-dadaa90a10e2	a6cd8b69-b344-40b5-e053-2995a90a1321

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
65692-2052-1	Hand Sanitizer	10 mL in 1 BOTTLE, SPRAY	LIQUID	10		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
65692-2052	HAND SANITIZER LIQUID [RAINING ROSE, INC]	1	Legacy NDC, 1 package rows	20200530_a6cd8b69-b344-40b5-e053-2995a90a1321.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Hand Sanitizer
DENATONIUM BENZOATE
MALTODEXTRIN
WATER
PROPYLENE GLYCOL
ALOE VERA LEAF
GLYCERIN
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
65692-2052	65692-2052-1

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
DENATONIUM BENZOATE	4YK5Z54AT2	IACT
MALTODEXTRIN	7CVR7L4A2D	IACT
WATER	059QF0KO0R	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
GLYCERIN	PDC6A3C0OX	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
a6cd994a-a8a8-0ce1-e053-2995a90a2b55			a6cd8b69-b344-40b5-e053-2995a90a1321	2020-05-29	Warnings	Exact identifier spl id: a6cd994a-a8a8-0ce1-e053-2995a90a2b55 spl set id: a6cd8b69-b344-40b5-e053-2995a90a1321

Reported adverse events (FAERS/openFDA)#

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

Hand Sanitizer