Alcohol Hand Sanitizer

Manufacturer
Clean Sleek Corporation | Qingyuan Hodm Cosmetics Manufacturing Co., Ltd.
Effective date
2020-05-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:32:04

Label at a glance#

ProductAlcohol Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

to decrease bacteria on the skin that could cause disease recoomended for repeated use

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping for children under 6, use only under adult supervision not recommended for infants

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Uses

INDICATIONS & USAGE SECTION

  • to decrease bacteria on the skin that could cause disease
  • recoomended for repeated use

Warning

WARNINGS SECTION

For external use only: hands

Flammable, keep away from fire or flame

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

  • keep out of eyes. In cases of contact with eyes, flush thoroughly with water
  • Avoid contact with broken skin.
  • Do not inhale or ingest

STOP USE AND ASK A DOCTOR IF

OTC - STOP USE SECTION

irritation and redness develop

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a poison control center right away.

DIrections

DOSAGE & ADMINISTRATION SECTION

  • wet hands thoroughly with product and allow to dry without wiping
  • for children under 6, use only under adult supervision
  • not recommended for infants

Other information

OTHER SAFETY INFORMATION

Store bewteen 15-30C (59-86F)

Avoid freezing and excessive heat above 40C (104F)

INACTIVE INGREDIENT SECTION

Water, Triethanolamine, Carbomer, parfum, Tocopherylacetate (Vitamin E Acetate), Aloe Barbadensis leaf jiuce, Glycerin, CI19140, CI42090

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

250 mL NDC: 77328-002-01

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77328-00277328-002-01
77327-002

Ingredients#

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

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

Source Document#

Source XML · Source PDF

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
bf834605-3ea2-4549-e053-2a95a90ae32ca50ad405-9fac-2e49-e053-2995a90abe252021-04-09WarningsExact identifier
spl set id: a50ad405-9fac-2e49-e053-2995a90abe25

Reported adverse events (FAERS/openFDA)#

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