FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
E.CIS Cosmetic Co.,Ltd
Effective date
2020-05-25
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 23:28:46

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure13 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

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v..........................Antiseptic ActiveActive

Purpose

OTC - PURPOSE SECTION

Antiseptic

PurposePurpose

USE

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available. USEUSE

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

Do not useDo not use▪in children less than 2 months of age

▪on open skin wounds

When using this product

OTC - WHEN USING SECTION

When usingWhen usingWhen using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

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

Keep out of reah of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep outKeep outKeep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

DirectionDirection• 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)

Other InformationOther Information

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Fragrance(Parfum), PEG-40 Hydrogenated Castor Oil, PEG-60 Hydrogenated Castor Oil, Scutellaria Baicalensis Root Extract,Portulaca Oleracea Extract, Aloe Barbadensis Leaf Extract Inactive ingredientsInactive ingredients

Questions or Comments?

OTC - QUESTIONS SECTION

Questions or CommentsQuestions or Comments1-800-819-4159

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EPU INSTANT HAND SANITIZER MIST NON-STERILE SOLUTION Help Reduce Bacteria On The Skin.
For all day use, No Sticky, Widely Spray, 100 mL (3.38 fl. oz.) PDPPDP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73862-101-132025-06-18C16284748780-1d6a99b39-a748-a426-e053-dadaa90af4c2HAND SANITIZER MIST 100ml
73862-101-132022-01-28C16284748780-1d6a99b39-a748-a426-e053-dadaa90af4c2HAND SANITIZER MIST 100ml

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73862-101HAND SANITIZER (ETHYL ALCOHOL) LIQUID [E.CIS COSMETIC CO.,LTD]6Legacy NDC20200528_a1f95631-d5fb-53c4-e053-2995a90acf8f.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73862-10173862-101-11, 73862-101-13

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
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
POLYOXYL 60 HYDROGENATED CASTOR OIL02NG325BQGIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
PURSLANEM6S840WXG5IACT
SCUTELLARIA BAICALENSIS ROOT7J95K7ID2SIACT

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
371a9c73-b26a-a65a-e063-6394a90af82aa1f95631-d5fb-53c4-e053-2995a90acf8f2025-06-08WarningsExact identifier
spl set id: a1f95631-d5fb-53c4-e053-2995a90acf8f

Reported adverse events (FAERS/openFDA)#

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