Hand Sanitizer

Manufacturer: Larry (Xiamen)Hi-Tech Co.,Ltd.
Effective date: 2020-04-13
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:06:20

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL, PHENOXYETHANOL, BENZYL ALCOHOL

Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Dosage

INACTIVE INGREDIENT SECTION

Inactive Ingredient

INDICATIONS & USAGE SECTION

Indication&Usage

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of children

OTC - PURPOSE SECTION

Purpose

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

WARNINGS SECTION

Warning

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand Sanitizer

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
BENZYL ALCOHOL Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73166-602-01	2022-01-28	C162847	48780-1	d6a99b39-3a41-a426-e053-dadaa90af4c2	a33b90b1-1c52-0fd3-e053-2995a90a47f5
73166-602-02	2022-01-28	C162847	48780-1	d6a99b39-3a41-a426-e053-dadaa90af4c2	a33b90b1-1c52-0fd3-e053-2995a90a47f5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73166-602-01	Hand Sanitizer	120 mL in 1 BOTTLE, PLASTIC	GEL	120		2
73166-602-02	Hand Sanitizer	250 mL in 1 BOTTLE, PLASTIC	GEL	250		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73166-602	HAND SANITIZER GEL [LARRY (XIAMEN)HI-TECH CO.,LTD.]	2	Legacy NDC, 2 package rows	20200415_a33b90b1-1c52-0fd3-e053-2995a90a47f5.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Hand Sanitizer
GLYCERIN
ALCOHOL
PHENOXYETHANOL
BENZYL ALCOHOL
POLYOXYL 40 HYDROGENATED CASTOR OIL
SODIUM HYDROXIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73166-602	73166-602-01, 73166-602-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
ALCOHOL	3K9958V90M	ACTIB
PHENOXYETHANOL	HIE492ZZ3T	ACTIB
BENZYL ALCOHOL	LKG8494WBH	ACTIB
POLYOXYL 40 HYDROGENATED CASTOR OIL	7YC686GQ8F	IACT
SODIUM HYDROXIDE	55X04QC32I	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
a33ba86a-a7e7-741c-e053-2995a90aa15e			a33b90b1-1c52-0fd3-e053-2995a90a47f5	2020-04-13	Warnings	Exact identifier spl id: a33ba86a-a7e7-741c-e053-2995a90aa15e spl set id: a33b90b1-1c52-0fd3-e053-2995a90a47f5

Reported adverse events (FAERS/openFDA)#

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