FDA.reportPublic FDA data

85279-002 Alcohol Sanitizer Spray

Manufacturer
Guangdong bangze medicine co., ltd
Effective date
2026-01-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:33:29

Label at a glance#

ProductAlcohol 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 below 106°F (41°C) ●May discolor certain fabrics or surfaces ●Validity period after opening: 12 months

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 60%.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Use(s) Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

●in children less than 2 months of age
●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.

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.
●Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

●Store below 106°F (41°C)
●May discolor certain fabrics or surfaces
●Validity period after opening: 12 months

Inactive ingredients

INACTIVE INGREDIENT SECTION

Sterile Distilled Water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1367692ethanol 60 % Topical SprayPSN3
1367692ethanol 0.6 ML/ML Topical SpraySCD3
1367692ethanol 60 % Topical SpraySY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85279-002-01Alcohol Sanitizer20 mL in 1 BOTTLESPRAY203

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85279-00285279-002-01

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
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
Alcohol SanitizerALCOHOL SANITIZER SPRAYGuangdong bangze medicine co., ltd2e9db49b-35ce-00d5-e063-6294a90acf352026-01-14WarningsExact identifier
ndc (package): 85279-002-01
ndc (product): 85279-002
ndc11 (package): 85279000201
spl id: 4854fccb-5ee6-119e-e063-6294a90abf7c
spl set id: 2e9db49b-35ce-00d5-e063-6294a90acf35

Reported adverse events (FAERS/openFDA)#

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