FDA.reportPublic FDA data

anti-bacterial hand sparay

Manufacturer
COSBE LABORATORY INC
Effective date
2021-05-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:44:59

Label at a glance#

Productanti-bacterial hand sparay
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Directions Spray on hands thoroughly andru bunt dry.

Storage and handling

May discolor certain fabrics or surf ces. Do not store above 110°F(43°C).

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%V/V.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Use to help reduce bac tera on skin

Warnings

WARNINGS SECTION

Flammable.Keep away from fire, flame and high heat.
For external use only.

Do not use

OTC - DO NOT USE SECTION

Do not inhale or ingest.

OTC - WHEN USING SECTION

When using this product, avoid contact with eyes.If contact occurs, rinse thorough with water.Avoid contact with broken skin.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets.If swallowed, get medical help or contact Poison

Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions Spray on hands thoroughly andru bunt dry.

Other information

STORAGE AND HANDLING SECTION

May discolor certain fabrics or surf ces.
Do not store above 110°F(43°C).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua) , Glycerin, Butylene Glycol, Fragrance(Parfumn) ,
Aloe Barbadensis Leaf Extract, Artemisia Argyi Leaf Extract, Cnidium Monnieri Fruit Extract, Sargassum Fusiforme Extract

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

74620-048-01 56ml

74620-048-01 56ml74620-048-01 56ml

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
74620-04874620-048-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
ALOE VERA LEAFZY81Z83H0XIACT
ARTEMISIA ARGYI LEAF2JYC99Q0WZIACT
SARGASSUM FUSIFORMEX436TJ4A11IACT
CNIDIUM MONNIERI FRUITV1IA3S3CUSIACT

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
f1544aba-dccb-2b2b-e053-2995a90af07ac21e718c-b848-a4fe-e053-2a95a90a70f82023-01-02WarningsExact identifier
spl set id: c21e718c-b848-a4fe-e053-2a95a90a70f8

Reported adverse events (FAERS/openFDA)#

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