Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure12 sections

Dosage and administration

wet hands thoroughly with product briskly rub hands together until dry supervise children under 6 years in the use of this product

Storage and handling

store at 20°C to 25°C(68° to 77°F) may discolor certain fabrics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v.

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on the skin

recommended for repeated use

Warnings

WARNINGS SECTION

For external use only
Flammable, keep away from heat and flame.

Do not use

OTC - DO NOT USE SECTION

Do not use in the eyes In case of contact rinse eyes thoroughly with wafer

OTC - WHEN USING SECTION

/

OTC - STOP USE SECTION

Stop use, and ask a doctor if irritation and redness develop and persistfor more than 72 hours.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product briskly rub hands together until dry
supervise children under 6 years in the use of this product

Other information

STORAGE AND HANDLING SECTION

store at 20°C to 25°C(68° to 77°F)
may discolor certain fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Aloe Vera, Trithanolamine, Vitamine E

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1

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
58503-801-01	2024-01-30	C162847	48780-1	1030e364-fdea-111a-e063-dadaa90a10e2	Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
58503-801-01	Hand Sanitizer	59 mL in 1 BOTTLE	GEL	59		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
58503-801	HAND SANITIZER GEL [CHINA NINGBO SHANGGE COSMETIC TECHNOLOGY CORP.]	1	Legacy NDC, 1 package rows	20200611_a7b7bada-ade4-670f-e053-2995a90a3579.zip

Products#

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

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

Hand Sanitizer
ALOE VERA LEAF
GLYCERIN
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
WATER
ALCOHOL
TROLAMINE
.ALPHA.-TOCOPHEROL SUCCINATE, D-

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
58503-801	58503-801-01

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
ALOE VERA LEAF	ZY81Z83H0X	IACT
GLYCERIN	PDC6A3C0OX	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
TROLAMINE	9O3K93S3TK	IACT
.ALPHA.-TOCOPHEROL SUCCINATE, D-	LU4B53JYVE	IACT

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
a7b7bf1c-43f3-1b14-e053-2a95a90a1052			a7b7bada-ade4-670f-e053-2995a90a3579	2020-06-09	Warnings	Exact identifier spl id: a7b7bf1c-43f3-1b14-e053-2a95a90a1052 spl set id: a7b7bada-ade4-670f-e053-2995a90a3579

Reported adverse events (FAERS/openFDA)#

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

Hand Sanitizer