FDA.reportPublic FDA data

UZO Hand Sanitizer

Manufacturer
ANTHOS GROUP, INC, THE
Effective date
2024-02-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:08:49

Label at a glance#

ProductUZO Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough Product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-20C(59-86F) Avoid freezing and excessive heat about 40C(104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentiaily can cause disease. for use when soap and water are not available.

Warnings

WARNINGS SECTION

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

Do not use
in children less than 2 months of age
on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs.
These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Do not use

OTC - DO NOT USE SECTION

Do not use
in children less than 2 months of age
on open skin wounds

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs.
These may be signs of a serious condition.

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs.
These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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

Place enough Product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

Store between 15-20C(59-86F)
Avoid freezing and excessive heat about 40C(104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, Glycerin, Carbomer, Aminomethyl Propanol, Parfum, Aloe Leaf Extract

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

79740-005-01 240ml79740-005-01 240ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN2
582753ethanol 0.7 ML/ML Topical SolutionSCD2
582753ethanol 70 % Topical SolutionSY2
582753ethyl alcohol 70 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79740-005-012025-07-29C16284748780-1d6a99b39-490b-a426-e053-dadaa90af4c279740-005 信息更新 UZO Hand Sanitizer
79740-005-012024-02-20C16284748780-1d6a99b39-490b-a426-e053-dadaa90af4c279740-005 信息更新 UZO Hand Sanitizer
79740-005-012022-01-28C16284748780-1d6a99b39-490b-a426-e053-dadaa90af4c279740-005 信息更新 UZO Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79740-005-01UZO Hand Sanitizer240 mL in 1 BOTTLELIQUID2402

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79740-005UZO HAND SANITIZER (HAND SANITIZER) LIQUID [ANTHOS GROUP, INC, THE]2Legacy NDC, 1 package rows20240221_b1c0a0d3-790a-3c04-e053-2995a90aadb4.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79740-00579740-005-01

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
NameUNIIKind
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
ALOE VERA LEAFZY81Z83H0XIACT
METHYL BENZOATE6618K1VJ9TIACT
AMINOMETHYLPROPANOLLU49E6626QIACT

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
11cc0183-1bc5-9ca9-e063-6294a90a4dbcb1c0a0d3-790a-3c04-e053-2995a90aadb42024-02-20WarningsExact identifier
spl id: 11cc0183-1bc5-9ca9-e063-6294a90a4dbc
spl set id: b1c0a0d3-790a-3c04-e053-2995a90aadb4

Reported adverse events (FAERS/openFDA)#

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