FDA.reportPublic FDA data

Advanced HAND SANITIZER

Manufacturer
COSBE LABORA TORY INC.
Effective date
2020-09-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:13:43

Label at a glance#

ProductAdvanced HAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

instant hand sanitizer gel kills 99.99% of germs use wherever and whenever without water squeeze thumbnail size amount in your palm then rub hands until dry.

Storage and handling

store below 110°F(43°C) may discolour certain fabric or surtaces

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62.5%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Use hand sanitizer to help reduce bacteia on the skin

Warnings

WARNINGS SECTION

Highly flammable.
Keep away fromfire or flame.
For external use only

OTC - DO NOT USE SECTION

/

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes
In case of contact with eyes or mouth, rinse with plenty of water and seek medical advice

OTC - STOP USE SECTION

/

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children
Children should use under adult supervision

Directions

DOSAGE & ADMINISTRATION SECTION

instant hand sanitizer gel kills 99.99% of germs
use wherever and whenever without water
squeeze thumbnail size amount in your palm then rub hands until dry.

Other information

STORAGE AND HANDLING SECTION

store below 110°F(43°C)
may discolour certain fabric or surtaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

acrylates/c10-30 alkyl acrylate crosspolymer,
aloe barbadensis leafextract,
artemisia argyi leaf extract,
butylene glycol
cnidium monnieri fruit extract,
glycerin,
sargassum fusiforme extract,
triethanolamine,
water(aqua)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC NO. 74620-007-01NDC NO. 74620-007-01

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74620-007-012023-01-03C16284748780-1d6a99b39-fc6b-a426-e053-dadaa90af4c274620-007 Advanced HAND SANITIZER
74620-007-012022-01-28C16284748780-1d6a99b39-fc6b-a426-e053-dadaa90af4c274620-007 Advanced HAND SANITIZER

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
74620-00774620-007-01

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
CNIDIUM MONNIERI FRUITV1IA3S3CUSIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
TROLAMINE9O3K93S3TKIACT
ALCOHOL3K9958V90MACTIB
SARGASSUM FUSIFORMEX436TJ4A11IACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
ARTEMISIA ARGYI LEAF2JYC99Q0WZIACT

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
f156bf54-6a95-2607-e053-2995a90abb67abc9712a-5e3e-c863-e053-2995a90a4fb52023-01-03WarningsExact identifier
spl set id: abc9712a-5e3e-c863-e053-2995a90a4fb5

Reported adverse events (FAERS/openFDA)#

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