FDA.reportPublic FDA data

Instant Hand Sanitizer

Manufacturer
COSBE LABORATORY INC.
Effective date
2020-04-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:36:59

Label at a glance#

ProductInstant Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

INSTANT HAND SANITIZER GEL KILLS 99.99% OF GERMS.USE WHEREVER AND WHENEVER WITHOUT WATER.PUMP PRODUCT IN PALM OF HAND AND RUB THOROUGHLY UNTIL HANDS ARE DRY.

Storage and handling

STORE BEL0W 110°F( 43°C). MAY DISCOLOUR CERTAIN FABRIC OR SURFACES.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 70-75%VN.

Purpose

OTC - PURPOSE SECTION

ANTIMICROBIAL

Use

INDICATIONS & USAGE SECTION

HAND SANITIZER TO HELP REDUCE BACTERIA ON THE SKIN.

Warnings

WARNINGS SECTION

HIGHLY FLAMMABLE KEEP AWAY FROM FIRE OR FLAME.FOR EXTERNAL USE ONLY, KEEP OUT OF THE REACH

OF CHILDREN. IN CASE OF EYE CONTACT, FLUSH WITH WATER. AVOID CONTACT WITH EYES. IN CASE OF CONTACT

WITH EYES OR MOUTH, RINSE WITH PLENTY OF WATER AND SEEK MEDICAL ADVICE. FOR CHILDREN,USE UNDER ADULT SUPERVISION.

Directions

DOSAGE & ADMINISTRATION SECTION

INSTANT HAND SANITIZER GEL KILLS 99.99% OF GERMS.USE WHEREVER AND WHENEVER WITHOUT WATER.PUMP

PRODUCT IN PALM OF HAND AND RUB THOROUGHLY UNTIL HANDS ARE DRY.

Other information

STORAGE AND HANDLING SECTION

STORE BEL0W 110°F( 43°C).

MAY DISCOLOUR CERTAIN FABRIC OR SURFACES.

Inactive ingredients

INACTIVE INGREDIENT SECTION

ALCOHOL, AQUA, GLYCERIN, BUTYLENE GLYCOL, ALOE BARBADENSIS EXTRACT, ARTEMISIA ARGYI LEAF

EXTRACT CNIDIUM MONNIERI EXTRACT, SARGASSUM FUSIFORME EXTRACT, CARBOMER,TRIETHANOLAMINE, FRAGRANCE.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60 ml label60 ml label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74620-002-012023-01-03C16284748780-1d6a99b39-6f4c-a426-e053-dadaa90af4c2a2b3beb4-a096-3ea5-e053-2a95a90accba
74620-002-012022-01-28C16284748780-1d6a99b39-6f4c-a426-e053-dadaa90af4c2a2b3beb4-a096-3ea5-e053-2a95a90accba

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74620-00274620-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ARTEMISIA ARGYI LEAF2JYC99Q0WZIACT
CNIDIUM MONNIERI FRUITV1IA3S3CUSIACT
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
FRAGRANCE LAVENDER & CHIA F-153480SXS9CO2TZKIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
SARGASSUM FUSIFORMEX436TJ4A11IACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT

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
f1571325-c928-5108-e053-2995a90a3bc8a2b3beb4-a096-3ea5-e053-2a95a90accba2023-01-03WarningsExact identifier
spl set id: a2b3beb4-a096-3ea5-e053-2a95a90accba

Reported adverse events (FAERS/openFDA)#

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