FDA.reportPublic FDA data

ANTI-BACTERIAL HAND SANITIZER

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 22:44:58

Label at a glance#

ProductANTI-BACTERIAL HAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Dispense into hand, rub thoroughtidry.

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

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product, avoid contact with eyes.If contact occurs, rinse thoroughwater.Avoid

contact wbroken skin.Do not inhale or ingest.

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

Dispense into hand, rub thoroughtidry.

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, Fagance (Parfum) , Acrylates/C10-30 Alkyl Acrylate crosspolymer, Triethanolamine, 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

74620-045-01 236ml

74620-045-01 236ml74620-045-01 236ml

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74620-04574620-045-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
TROLAMINE9O3K93S3TKIACT
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
f154605c-5013-05bb-e053-2995a90a5fc7c21e077a-98ad-4bce-e053-2995a90a6d072023-01-02WarningsExact identifier
spl set id: c21e077a-98ad-4bce-e053-2995a90a6d07

Reported adverse events (FAERS/openFDA)#

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