HAND SANITISER

Manufacturer
Jiangxi Iris Chemical Co.,Ltd
Effective date
2020-05-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:11:01

Label at a glance#

ProductHAND SANITISER
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough product on hands to cover all surfaces.Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30C(59-86F). Avoid freezing and excessive heat above 40C(104F).

Label contents#

Full prescribing information#

Active ingredient[s]

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use[s]

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease.

For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only.Flammable.Keep away from heat or flame.

Do not use

OTC - DO NOT USE SECTION

in children less than 2 months of age

on open skin wounds

When using this product

OTC - WHEN USING SECTION

keep out of eyes,ears, and mouth.In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs.These may be signs of a serious condition.

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

Place enough product on hands to cover all surfaces.Rub hands together until dry.

Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

Store between 15-30C(59-86F).

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua) ,Carbomer,Triethanolamine,Tocopheryl Acetate.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60 ml label60 ml label100 ml label100 ml label250 ml label250 ml label500 ml label500 ml label1000 ml label1000 ml label

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#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74440-013-01HAND SANITISER60 mL in 1 BOTTLEGEL602
74440-013-02HAND SANITISER100 mL in 1 BOTTLEGEL1002
74440-013-03HAND SANITISER250 mL in 1 BOTTLEGEL2502
74440-013-04HAND SANITISER500 mL in 1 BOTTLEGEL5002
74440-013-05HAND SANITISER1000 mL in 1 BOTTLEGEL10002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74440-013HAND SANITISER GEL [JIANGXI IRIS CHEMICAL CO.,LTD]2Legacy NDC, 5 package rows20200513_a56f9127-f17a-3d19-e053-2995a90ab414.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
74440-01374440-013-01, 74440-013-02, 74440-013-03, 74440-013-04, 74440-013-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
a56f9127-f176-3d19-e053-2995a90ab414a56f9127-f17a-3d19-e053-2995a90ab4142020-05-12WarningsExact identifier
spl id: a56f9127-f176-3d19-e053-2995a90ab414
spl set id: a56f9127-f17a-3d19-e053-2995a90ab414

Reported adverse events (FAERS/openFDA)#

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