FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
Guangdong Boxi High-Tech Co., Ltd.
Effective date
2020-05-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:29:22

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry. Children under 6 years of age should be supervised when using this product.

Storage and handling

Store below30°C(86°F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80.0%V/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on skin

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

do not use in or near the eyes

OTC - WHEN USING SECTION

When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water

OTC - STOP USE SECTION

Stop use and ask doctor if irritation or rash appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach for childrenIf swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry.
Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

Store below30°C(86°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua), Glycerin, Hydrogen peroxide

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

88

22229933191915151616111100111212141420205513131010171777442221211818232366

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75702-00875702-008-01, 75702-008-02, 75702-008-03, 75702-008-04, 75702-008-05, 75702-008-06, 75702-008-07, 75702-008-08, 75702-008-09, 75702-008-10, 75702-008-11, 75702-008-12, 75702-008-13, 75702-008-14, 75702-008-15, 75702-008-16, 75702-008-17, 75702-008-18, 75702-008-19, 75702-008-20, 75702-008-21, 75702-008-22, 75702-008-23, 75702-008-24

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
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
b962d785-a648-b6d3-e053-2995a90a9347a5ace2cd-5c87-2fec-e053-2a95a90a5ce12021-01-21WarningsExact identifier
spl set id: a5ace2cd-5c87-2fec-e053-2a95a90a5ce1

Reported adverse events (FAERS/openFDA)#

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