FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Guangzhou Boss Biological Technique Ltd.
Effective date
2020-05-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:14:10

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 below 06 F(41°C). May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on skin

Warnings

WARNINGS SECTION

Flammable, Keep away from fire or flame.
For external use only.

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. Stop use and ask doctor if irritation or rash appears and lasts.
Keep out of reach for children.
If swallowed, get medical help or contact a Poison Control Center right away.

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 children.
If 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 below 06 F(41°C).
May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerol, Sophora Flavescens Extract, Aloe VeraExtract, Carbomer, Triethanolamine

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

07070505010102020808060603030404

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047755ethanol 75 % Topical SolutionPSN1
1047755ethanol 0.75 ML/ML Topical SolutionSCD1
1047755ethanol 75 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76762-006-012021-07-23C16284748780-1c7ccaba7-1ce9-fd44-e053-dadaa90aa01bHand Sanitizer
76762-006-022021-07-23C16284748780-1c7ccaba7-1ce9-fd44-e053-dadaa90aa01bHand Sanitizer
76762-006-032021-07-23C16284748780-1c7ccaba7-1ce9-fd44-e053-dadaa90aa01bHand Sanitizer
76762-006-042021-07-23C16284748780-1c7ccaba7-1ce9-fd44-e053-dadaa90aa01bHand Sanitizer
76762-006-052021-07-23C16284748780-1c7ccaba7-1ce9-fd44-e053-dadaa90aa01bHand Sanitizer
76762-006-062021-07-23C16284748780-1c7ccaba7-1ce9-fd44-e053-dadaa90aa01bHand Sanitizer
76762-006-072021-07-23C16284748780-1c7ccaba7-1ce9-fd44-e053-dadaa90aa01bHand Sanitizer
76762-006-082021-07-23C16284748780-1c7ccaba7-1ce9-fd44-e053-dadaa90aa01bHand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76762-006-01Hand Sanitizer30 mL in 1 BOTTLELIQUID301
76762-006-02Hand Sanitizer50 mL in 1 BOTTLELIQUID501
76762-006-03Hand Sanitizer100 mL in 1 BOTTLELIQUID1001
76762-006-04Hand Sanitizer200 mL in 1 BOTTLELIQUID2001
76762-006-05Hand Sanitizer250 mL in 1 BOTTLELIQUID2501
76762-006-06Hand Sanitizer300 mL in 1 BOTTLELIQUID3001
76762-006-07Hand Sanitizer500 mL in 1 BOTTLELIQUID5001
76762-006-08Hand Sanitizer1000 mL in 1 BOTTLELIQUID10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76762-006HAND SANITIZER LIQUID [GUANGZHOU BOSS BIOLOGICAL TECHNIQUE LTD.]1Legacy NDC, 8 package rows20200522_a598ed29-a5d1-0b3a-e053-2995a90a29a8.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76762-00676762-006-01, 76762-006-02, 76762-006-03, 76762-006-04, 76762-006-05, 76762-006-06, 76762-006-07, 76762-006-08

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
NameUNIIKind
TROLAMINE9O3K93S3TKIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
SOPHORA FLAVESCENS ROOTIYR6K8KQ5KIACT
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a5991163-7849-dc5a-e053-2995a90ab9b5a598ed29-a5d1-0b3a-e053-2995a90a29a82020-05-14WarningsExact identifier
spl id: a5991163-7849-dc5a-e053-2995a90ab9b5
spl set id: a598ed29-a5d1-0b3a-e053-2995a90a29a8

Reported adverse events (FAERS/openFDA)#

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