FDA.reportPublic FDA data

QC 2OZ INSTANT HAND SANITIZER (ORIGINAL)

Manufacturer
Ningbo Liyuan Daily Chemical Products Co., Ltd.
Effective date
2018-05-21
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-02 00:57:37

Label at a glance#

ProductQC 2OZ INSTANT HAND SANITIZER (ORIGINAL)
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Wet hands thoroughly with product and rub until dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.

Label contents#

Full prescribing information#

Drug Facts Medicinal Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Features

INDICATIONS & USAGE SECTION

  • To decrease bacteria on the skin that could cause disease.
  • Recommended for repeated use.
  • Use anywhere without water.

Warning

WARNINGS SECTION

  • For external use only-hands
  • Flammable, keep away from heat and flame
  • Discontinue if skin becomes irritated and ask a doctor

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Posion Control Center immediately.

Non-Medicinal

INACTIVE INGREDIENT SECTION

Water, Isopropyl Alcohol, Glycerin, Carbomer, Aminomethyl Propanol, Parfum, Propylene Glycol, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and rub until dry without wiping.
For children under 6, use only under adult supervision.
Not recommended for infants.

When using this product

OTC - WHEN USING SECTION

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

Other information

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

  • Do not store above 105℉.
  • May discolor some fabrics.
  • Harmful to wood finishes and plastics.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76176-03476176-034-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
249618bf-76ff-f254-e063-6394a90a3f465b2df5de-32a6-3da2-e053-2991aa0a01c42018-12-31WarningsExact identifier
spl set id: 5b2df5de-32a6-3da2-e053-2991aa0a01c4

Reported adverse events (FAERS/openFDA)#

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