FDA.reportPublic FDA data

EAAE Disinfectant

Manufacturer
iHotel Guest Amenities Co.,Ltd
Effective date
2020-04-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:07:25

Label at a glance#

ProductEAAE Disinfectant
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Put enough products on your palm to cover hands and rub hands together briskly until dry

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% 

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only.

Non Medical. Flammable. Keep away from fire or flame

When using this product, do not use in or near eyes, In case of contact, rinse thoroughly with water

OTC - STOP USE SECTION

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 products on your palm to cover hands and rub hands together briskly until dry

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Carbomer, Triethanolamine, Glycerin, Perfume, Castor Oil, Hydrogenated, ethoxylated

60 mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

300 mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

500 mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN2
1305100ethanol 0.75 ML/ML Topical GelSCD2
1305100ethanol 75 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71004-101-012022-01-28C16284748780-1d6a99b39-d793-a426-e053-dadaa90af4c284ef2824-7461-455b-abf0-3846ffecd96b
71004-101-022022-01-28C16284748780-1d6a99b39-d793-a426-e053-dadaa90af4c284ef2824-7461-455b-abf0-3846ffecd96b
71004-101-032022-01-28C16284748780-1d6a99b39-d793-a426-e053-dadaa90af4c284ef2824-7461-455b-abf0-3846ffecd96b

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71004-101-01EAAE Disinfectant60 mL in 1 BOTTLEGEL602
71004-101-02EAAE Disinfectant300 mL in 1 BOTTLEGEL3002
71004-101-03EAAE Disinfectant500 mL in 1 BOTTLEGEL5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71004-101EAAE DISINFECTANT (ALCOHOL) GEL [IHOTEL GUEST AMENITIES CO.,LTD]2Legacy NDC, 3 package rows20200423_84ef2824-7461-455b-abf0-3846ffecd96b.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71004-10171004-101-01, 71004-101-02, 71004-101-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER 934Z135WT9208IACT
TRIETHANOLAMINE SULFATEMV1V89M17OIACT
GLYCERINPDC6A3C0OXIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
ALCOHOL3K9958V90MACTIB

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
a3e860c1-dce6-764e-e053-2a95a90ad00f84ef2824-7461-455b-abf0-3846ffecd96b2020-04-22WarningsExact identifier
spl id: a3e860c1-dce6-764e-e053-2a95a90ad00f
spl set id: 84ef2824-7461-455b-abf0-3846ffecd96b

Reported adverse events (FAERS/openFDA)#

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