FDA.reportPublic FDA data

EUNOS advanced hand sanitizer

Manufacturer
YIRONG TRADING (NANJING) CO., LTD
Effective date
2020-04-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:09:02

Label at a glance#

ProductEUNOS advanced hand sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin that could cause disease.

Dosage and administration

Put enough product in your palm to cover hands and rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product Other Information Store below 105℉(40℃). May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol Denat.70% v/v.

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin that could cause disease.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only

When using this product

  • do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
  • avoid using on broken skin.

Stop use and ask a doctor if irritation or rash appears and lasts

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

  • Put enough product in your palm to cover hands and rub hands together briskly until dry.
  • Children under 6 years of age should be supervised when using this product

Other Information

  • Store below 105℉(40℃).
  • May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Acrylates Copolymer, Propylene Glycol, Butylene Clycol, Aminomethyl Propanol

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60 mL Label

60 mL Label60 mL Label

100 mL Label

100 mL Label100 mL Label

500 mL Label

500 mL Label500 mL Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75007-001-012022-01-28C16284748780-1d6a99b39-f13a-a426-e053-dadaa90af4c21e0b67fd-9656-49d3-9831-7b50c2f4537e
75007-001-022022-01-28C16284748780-1d6a99b39-f13a-a426-e053-dadaa90af4c21e0b67fd-9656-49d3-9831-7b50c2f4537e
75007-001-032022-01-28C16284748780-1d6a99b39-f13a-a426-e053-dadaa90af4c21e0b67fd-9656-49d3-9831-7b50c2f4537e

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75007-001-01EUNOS advanced hand sanitizer60 mL in 1 BOTTLEGEL601
75007-001-02EUNOS advanced hand sanitizer100 mL in 1 BOTTLEGEL1001
75007-001-03EUNOS advanced hand sanitizer500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75007-001EUNOS ADVANCED HAND SANITIZER (ALCOHOL) GEL [YIRONG TRADING (NANJING) CO., LTD]1Legacy NDC, 3 package rows20200501_1e0b67fd-9656-49d3-9831-7b50c2f4537e.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75007-00175007-001-01, 75007-001-02, 75007-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW)JZ1374NL9EIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
AMINOMETHYLPROPANOLLU49E6626QIACT

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
38cdb853-d9fb-42a3-b0e0-9d198d4962b01e0b67fd-9656-49d3-9831-7b50c2f4537e2020-04-26WarningsExact identifier
spl id: 38cdb853-d9fb-42a3-b0e0-9d198d4962b0
spl set id: 1e0b67fd-9656-49d3-9831-7b50c2f4537e

Reported adverse events (FAERS/openFDA)#

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