Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure11 sections

Storage and handling

Store below 110°F (43°C)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethanol 70%. Purpose: Antimicrobial

Active Ingredient

Purpose

OTC - PURPOSE SECTION

Hand sanitizer to help decrease bacteria on the skin.

Use purpose

Use

INDICATIONS & USAGE SECTION

Spray enough product on hands to cover all surfaces. Rub hands together until hands feel dry.

Indicate & usage

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame For external use only.Highly falmmable liquids and vapors.

Fammable warningfammable

Do not use

OTC - DO NOT USE SECTION

Do not use in or near the eyes. If contact occurs, flush thoroughly with water.

Do not use.

OTC - STOP USE SECTION

Stop use and contact doctor if redness and irritation develops and persists.

Stop use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Keep out of children

Other information

STORAGE AND HANDLING SECTION

Store below 110°F (43°C)

Other info-storage

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (Water), Glycerin, Parfum (Fragrance), Aloe Barbadensis Leaf Extract.

Inactive ingredient

DOSAGE & ADMINISTRATION SECTION

Spray enough product on hands to cover all surfaces. Rub hands together until hands feel dry.

dosage & Admin

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pocket hand sanitizer

package label

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1041849	ethanol 0.7 ML/ML Topical Spray	ethanol 0.7 ML/ML Topical Spray	SCD Active

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1041849	ethanol 70 % Topical Spray	PSN	1
1041849	ethanol 0.7 ML/ML Topical Spray	SCD	1
1041849	ethanol 70 % Topical Spray	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
80380-070-01	2022-01-28	C162847	48780-1	d6a99b39-9707-a426-e053-dadaa90af4c2	b21e3dcc-7899-f35e-e053-2995a90a44cc

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
80380-070-01	Hand Sanitizer	70 mL in 1 CASE	SPRAY	70		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
80380-070	HAND SANITIZER (ALCOHOL) SPRAY [SHEDRAIN CORPORATION]	1	Legacy NDC, 1 package rows	20201023_b21e3dcc-7899-f35e-e053-2995a90a44cc.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Hand Sanitizer
ALCOHOL
GLYCERIN
ALOE VERA LEAF
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
80380-070	80380-070-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
ALOE VERA LEAF	ZY81Z83H0X	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
b21e3b78-1f60-65b8-e053-2995a90a8c9e			b21e3dcc-7899-f35e-e053-2995a90a44cc	2020-10-23	Warnings	Exact identifier spl id: b21e3b78-1f60-65b8-e053-2995a90a8c9e spl set id: b21e3dcc-7899-f35e-e053-2995a90a44cc

Reported adverse events (FAERS/openFDA)#

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

Hand Sanitizer