Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure11 sections

Dosage and administration

Rub hands thoroughlywith this product until dry, children younger than 6 should be supervised by an adult when using.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

hand sanitizer

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Effect:

INDICATIONS & USAGE SECTION

Hand sanitizer to decrease bacteria on the skin that could cause disease.

Warnings:

WARNINGS SECTION

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

When using this product

OTC - WHEN USING SECTION

avoid contacting with face, eyes, and broken skin. In case of eye contacting, flush with plenty of water and seek medical attention.

Stop use and consut a doctor if

OTC - STOP USE SECTION

irritation or redness occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions:

DOSAGE & ADMINISTRATION SECTION

Rub hands thoroughlywith this product until dry, children younger than 6 should be supervised by an adult when using.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Water (Aqua), Triethanolamine, Polyacrylic Adcid, Aloe Barbadensis (Aloe Vera) Gel, Glycerin, Propylence Glycol, Tocophery Acetate (Vitamin E).

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

UILAME 30ml

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1047755	ethanol 0.75 ML/ML Topical Solution	ethanol 0.75 ML/ML Topical Solution	SCD Active

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1047755	ethanol 75 % Topical Solution	PSN	1
1047755	ethanol 0.75 ML/ML Topical Solution	SCD	1
1047755	ethanol 75 % Topical Solution	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
77972-101-09	2021-07-23	C162847	48780-1	c7ccaba7-10b6-fd44-e053-dadaa90aa01b	hand sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
77972-101-09	Hand Sanitizer	30 mL in 1 BOTTLE	LIQUID	30		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77972-101	HAND SANITIZER (ALCOHOL) LIQUID [ZHEJIANG TAOYEL BIOLOGICAL TECHNOLOGY CO., LTD.]	1	Legacy NDC, 1 package rows	20200527_a698ea8f-cea9-004a-e053-2995a90ac312.zip

Products#

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

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

Hand Sanitizer
ALCOHOL
POLYACRYLIC ACID (250000 MW)
ALOE VERA LEAF
GLYCERIN
WATER
AMINOMETHYLPROPANOL
PROPYLENE GLYCOL
.ALPHA.-TOCOPHEROL ACETATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77972-101	77972-101-09

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
POLYACRYLIC ACID (250000 MW)	9G2MAD7J6W	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	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
a698cced-5fb4-17ea-e053-2a95a90a448c			a698ea8f-cea9-004a-e053-2995a90ac312	2020-06-01	Warnings	Exact identifier spl id: a698cced-5fb4-17ea-e053-2a95a90a448c spl set id: a698ea8f-cea9-004a-e053-2995a90ac312

Reported adverse events (FAERS/openFDA)#

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

Hand Sanitizer