Hand Sanitizer

Manufacturer: Guangzhou Zhongkebaishi Health Industry CO., LTD
Effective date: 2020-08-28
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: legacy-cache
Hydrated at: 2026-08-01 23:16:07

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure13 sections

Dosage and administration

Pump a small amount of gel into palm of hand Rub thoroughly over all surfaces of both bands Rub hands together briskly until dry

Storage and handling

Keep away from the direct sunlight Store at room temperature

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin

Recommended for repeated use

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

in children less than 2 years of age
on open skin wounds or if allergy to alcohol

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops or if condition persists for 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

Pump a small amount of gel into palm of hand

Rub thoroughly over all surfaces of both bands

Rub hands together briskly until dry

Other information

STORAGE AND HANDLING SECTION

Keep away from the direct sunlight

Store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Aloe Barbadense Leaf Extract, Carbomer, Triethanolamine

RECENT MAJOR CHANGES SECTION

Indications and Usage

Dosage and Administration

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

480 mL NDC: 73813-2011-1

PDP

50 mL NDC: 73813-2011-4

PDP

100 mL NDC: 73813-2011-5

PDP

236 mL NDC: 73813-2011-6

PDP

300 mL NDC: 73813-2011-7

PDP

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Hand Sanitizer
ALCOHOL
ALOE VERA LEAF
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
WATER
TROLAMINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73813-2011	73813-2011-1, 73813-2011-3, 73813-2011-4, 73813-2011-5, 73813-2011-6, 73813-2011-7

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALOE VERA LEAF	ZY81Z83H0X	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
WATER	059QF0KO0R	IACT
TROLAMINE	9O3K93S3TK	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML · Source PDF

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
bae1cef2-e486-ab0e-e053-2995a90a2066			a2015b60-38e4-2688-e053-2995a90a618d	2021-02-09	Warnings	Exact identifier spl set id: a2015b60-38e4-2688-e053-2995a90a618d

Reported adverse events (FAERS/openFDA)#

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