80598-001 DISINFECTANT SPRAY

Manufacturer
Aiyinuo Technology Co., Ltd.
Effective date
2020-09-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:30:16

Label at a glance#

ProductDISINFECTANT
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

l.Hand disinfection:follow the standard method to use soap to wash hands ,rinse with running water,dry with sterile towels,then direct spray this product on hands and fore-arms until moist wait for 3 minutes,rub hands until dry. General object surface disinfection: directly spray on the object surface for until moist,wait for 3-Sminutes.

Storage and handling

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Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethanol 75%(v/v)

Purpose

OTC - PURPOSE SECTION

Efficient to kill Staphylococcus aureus,E.coli Pseudo-monas aeruginosa and Candida albicans etc.

Use

INDICATIONS & USAGE SECTION

Hand disinfection,general object surface disin-fection.

Warnings

WARNINGS SECTION

l.EXTREMELY FLAMMABLE.
Pressurized container; protect from sunlight and don't expose to temperatres exceeding S0°C.Don' t pierce or bum, even after use. Don't spray on a naked flame or any incandescent material. Keep it away from the reach of children. Don't spray towards eyes.
2.External disinfectant shuold not be taken orally and kept out of reach of children.
3.Use with caution if allergic to alcohol.
4.lt should not be used to disinfect fat-soluble surfaces.
5.This product is irritating to wounds and mucous mem-branes.

Do not use

OTC - DO NOT USE SECTION

Pressurized container; protect from sunlight and don't expose to temperatres exceeding S0°C.Don' t pierce or bum, even after use. Don't spray on a naked flame or any incandescent material. Keep it away from the reach of children. Don't spray towards eyes.

OTC - WHEN USING SECTION

External disinfectant shuold not be taken orally and kept out of reach of children.
Use with caution if allergic to alcohol.
lt should not be used to disinfect fat-soluble surfaces.
This product is irritating to wounds and mucous mem-branes.

OTC - STOP USE SECTION

/

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

External disinfectant shuold not be taken orally and kept out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

l.Hand disinfection:follow the standard method to use soap to wash hands ,rinse with running water,dry with sterile towels,then direct spray this product on hands and fore-arms until moist wait for 3 minutes,rub hands until dry.
General object surface disinfection: directly spray on the object surface for until moist,wait for 3-Sminutes.

Other information

STORAGE AND HANDLING SECTION

/

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water 24.7%, Aloe essence 0.3%

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

80598-001-04 160ml80598-001-04 160ml80598-001-05 300ml80598-001-05 300ml80598-001-03 120ml80598-001-03 120ml80598-001-01 75ml80598-001-01 75ml80598-001-06 500ml80598-001-06 500ml80598-001-02 100ml80598-001-02 100ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286295ethanol 75 % Topical SprayPSN1
2286295ethanol 0.75 ML/ML Topical SpraySCD1
2286295ethanol 75 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80598-001-01DISINFECTANT75 mL in 1 BOTTLESPRAY751
80598-001-02DISINFECTANT100 mL in 1 BOTTLESPRAY1001
80598-001-03DISINFECTANT120 mL in 1 BOTTLESPRAY1201
80598-001-04DISINFECTANT160 mL in 1 BOTTLESPRAY1601
80598-001-05DISINFECTANT300 mL in 1 BOTTLESPRAY3001
80598-001-06DISINFECTANT500 mL in 1 BOTTLESPRAY5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80598-001DISINFECTANT (DISINFECTANT SPRAY) SPRAY [AIYINUO TECHNOLOGY CO., LTD.]1Legacy NDC, 6 package rows20200926_b01c0d09-2cd7-95ef-e053-2995a90a1c16.zip

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
80598-00180598-001-01, 80598-001-02, 80598-001-03, 80598-001-04, 80598-001-05, 80598-001-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOEV5VD430YW9IACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
b01c0d09-2cc9-95ef-e053-2995a90a1c16b01c0d09-2cd7-95ef-e053-2995a90a1c162020-09-24WarningsExact identifier
spl id: b01c0d09-2cc9-95ef-e053-2995a90a1c16
spl set id: b01c0d09-2cd7-95ef-e053-2995a90a1c16

Reported adverse events (FAERS/openFDA)#

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