FDA.reportPublic FDA data

antibacterial hand sanitizer

Manufacturer
Cosmuses Cosmetics (Ningbo) Co., Ltd.
Effective date
2024-06-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:59:51

Label at a glance#

Productantibacterial hand sanitizer 01
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

For hand Sanitizing

Dosage and administration

Wet hands throughly with product and allow to dry without wiping. For children under 6 age use only under adult supervision. Not recommended for infants.

Storage and handling

Other information ​ Do not store above 105 o F. May discolor some fabrics.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • For hand Sanitizing

Warnings

WARNINGS SECTION

For external use only- hands.

Flammable. Keep away from heat and flame.

OTC - WHEN USING SECTION

When using this product, keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.

OTC - STOP USE SECTION

Stop use and ask doctor if irritation develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or call a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands throughly with product and allow to dry without wiping.
  • For children under 6 age use only under adult supervision.
  • Not recommended for infants.

STORAGE AND HANDLING SECTION

Other information ​

  • Do not store above 105 oF.
  • May discolor some fabrics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aqua, Glycerin, Propylene Glycol, Aloe Barbadensis Leaf Extract, Carbomer, Triethanolamine, Tocopheryl Acetate, Fragrance, PEG-40 Hydrogenated Castor Oil.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

82953-01482953-014

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
82953-01482953-014-02, 82953-014-05, 82953-014-03, 82953-014-06, 82953-014-07, 82953-014-04, 82953-014-08, 82953-014-01, 82953-014-09, 82953-014-10

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
FRAGRANCE 135765EM498GW35IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
CARBOMER 9404Q93RCW27EIACT
TROLAMINE9O3K93S3TKIACT
ALCOHOL3K9958V90MACTIB
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT

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
1c26aedd-8c6a-382c-e063-6394a90adabc19a43c79-0b30-7c00-e063-6394a90acdd82024-06-30WarningsExact identifier
spl id: 1c26aedd-8c6a-382c-e063-6394a90adabc
spl set id: 19a43c79-0b30-7c00-e063-6394a90acdd8

Reported adverse events (FAERS/openFDA)#

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