FDA.reportPublic FDA data

ANTI-BACTERIAL HAND SANITIZER

Manufacturer
COSBE LABORATORY INC
Effective date
2021-02-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:38:32

Label at a glance#

ProductANTI-BACTERIAL HAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Dispense into hands, rub until dry.

Storage and handling

May discolor certain fabrics or surfaces. Oo not stor above 110F (43C)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% V/V

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Use to help reduce bacteria on skin

Warnings

WARNINGS SECTION

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

When using this product ,avoid contact with eyes. If contact occurs, rinse thoroughly with water. Avoid contact with brokern skin.
Do not inhale or ingest.

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

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

OTC - DO NOT USE SECTION

/

When using this product

OTC - WHEN USING SECTION

When using this product ,avoid contact with eyes. If contact occurs, rinse thoroughly with water. Avoid contact with brokern skin.
Do not inhale or ingest.

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

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

OTC - STOP USE SECTION

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

Keep out of reach of children

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 hands, rub until dry.

Other information

STORAGE AND HANDLING SECTION

May discolor certain fabrics or surfaces. Oo not stor above 110F (43C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua), Glycerin, Butylene Glycol, Fagrance(Parfum), Acrylates/C10-30Alkyl Acrylate Crosspolymer, Triethanolamine, Aloe Barbadensis Leaf Extract, Artemisia Argyi Leaf Extract, Cnidium Monnieri Frut Extrac, Sargassum Fusiforme Extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

74620-039-01 236ml 74620-039-01 236ml74620-039-01 236ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74620-039-012023-01-30C16284748780-1f386c649-c2ed-0266-e053-dadaa90a7c1a74620-039 ANTI-BACTERIAL HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74620-039-01ANTI-BACTERIAL HAND SANITIZER236 mL in 1 BOTTLEGEL2361

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74620-039ANTI-BACTERIAL HAND SANITIZER GEL [COSBE LABORATORY INC]1Legacy NDC, 1 package rows20210225_bc10f4e1-52f6-1e0e-e053-2a95a90a81d0.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74620-03974620-039-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
TROLAMINE9O3K93S3TKIACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
FRAGRANCE CLEAN ORC0600327329LCV5BTFIACT
ALCOHOL3K9958V90MACTIB
SARGASSUM FUSIFORMEX436TJ4A11IACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
ARTEMISIA ARGYI LEAF2JYC99Q0WZIACT
CNIDIUM MONNIERI FRUITV1IA3S3CUSIACT
BUTYLENE GLYCOL3XUS85K0RAIACT

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
bc10f258-ce8e-1c10-e053-2a95a90a204fbc10f4e1-52f6-1e0e-e053-2a95a90a81d02021-02-24WarningsExact identifier
spl id: bc10f258-ce8e-1c10-e053-2a95a90a204f
spl set id: bc10f4e1-52f6-1e0e-e053-2a95a90a81d0

Reported adverse events (FAERS/openFDA)#

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