FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
YOSUN TECH. CO., LTD.
Effective date
2020-04-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:35:14

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

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

Storage and handling

Do not store above 105F May discolor some fabrics Harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Uses to decrease bacteria on the skin that could cause disease.

Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only: hands

Flammable, keep away from fire or flame

OTC - WHEN USING SECTION

When using this product keep out of eyes. In case of contact with eyes, flush eyes thoroughly with water.

Avoid contact with broken skin

Do not inhale or ingest

OTC - STOP USE SECTION

Stop use and ask a doctor

if irritation or redness develop

Condition persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact 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, use only with adult supervision
  • Not reccomended for infants

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, glycerin, Grape Seed Extract, Carbomer, PEG-40 Hydrogented Castor Oil, Sodium Hydroxide, Fragrance.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front and Back LabelFront and Back Label80 mL NDC: 75604-001-80

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75604-00175604-001-80

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
FRAGRANCE LAVENDER & CHIA F-153480SXS9CO2TZKIACT
CARBOMER 1342809Y72KV36IACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
SODIUM HYDROXIDE55X04QC32IIACT
PEG-40 CASTOR OIL4ERD2076EFIACT
GRAPEFRUIT SEED OIL598D944HOLIACT

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
c19c2d80-dbed-3c6c-e053-2995a90a23c9a382aca9-168a-c3f2-e053-2995a90a633b2021-05-05WarningsExact identifier
spl set id: a382aca9-168a-c3f2-e053-2995a90a633b

Reported adverse events (FAERS/openFDA)#

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