79864-002 Sanitizing Spray

Manufacturer
guangdong leiqi cosmetic company ltd,.
Effective date
2021-01-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:36:57

Label at a glance#

ProductSanitizing
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Children under 6 years of age should be supervised when using this product.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F) 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

Antiseptic

Use

INDICATIONS & USAGE SECTION

Sanitizing spray to help reduce bacteria that potentially can cause disease. For use when soap and water are not available

Do not use

OTC - DO NOT USE SECTION

Do not use in children less than 2 months of age, nor on open skin wounds.

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 - STOP USE SECTION

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

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. Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)
May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

79864-002-02 60ML79864-002-02 60ML79864-002-03 100ML79864-002-03 100ML79864-002-08 1000ML79864-002-08 1000ML79864-002-09 2500ML79864-002-09 2500ML79864-002-04 200ML79864-002-04 200ML79864-002-05 250ML79864-002-05 250ML79864-002-01 30ML79864-002-01 30ML79864-002-10 5000ML79864-002-10 5000ML79864-002-07 500ML79864-002-07 500ML79864-002-06 300ML79864-002-06 300ML

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286295ethanol 75 % Topical SprayPSN2
2286295ethanol 0.75 ML/ML Topical SpraySCD2
2286295ethanol 75 % Topical SpraySY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79864-002-01Sanitizing30 mL in 1 BOTTLESPRAY302
79864-002-02Sanitizing60 mL in 1 BOTTLESPRAY602
79864-002-03Sanitizing100 mL in 1 BOTTLESPRAY1002
79864-002-04Sanitizing200 mL in 1 BOTTLESPRAY2002
79864-002-05Sanitizing250 mL in 1 BOTTLESPRAY2502
79864-002-06Sanitizing300 mL in 1 BOTTLESPRAY3002
79864-002-07Sanitizing500 mL in 1 BOTTLESPRAY5002
79864-002-08Sanitizing1000 mL in 1 BOTTLESPRAY10002
79864-002-09Sanitizing2500 mL in 1 BOTTLESPRAY25002
79864-002-10Sanitizing5000 mL in 1 BOTTLESPRAY50002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79864-002SANITIZING SPRAY [GUANGDONG LEIQI COSMETIC COMPANY LTD,.]2Legacy NDC, 10 package rows20210115_ac926138-12f9-5d34-e053-2995a90a8ee0.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
b8e8707d-c8ce-7930-e053-2995a90aa038ac926138-12f9-5d34-e053-2995a90a8ee02021-01-14WarningsExact identifier
spl id: b8e8707d-c8ce-7930-e053-2995a90aa038
spl set id: ac926138-12f9-5d34-e053-2995a90a8ee0

Reported adverse events (FAERS/openFDA)#

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