FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
E.CIS Cosmetic Co.,Ltd
Effective date
2020-05-29
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-01 23:28:26

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

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 70% v/v..........................Antiseptic

Active ingredientsActive ingredients

Purpose

OTC - PURPOSE SECTION

Purpose.Antiseptic

PurposePurpose

Use[s]

INDICATIONS & USAGE SECTION

Health care personnel hand rub to help reduce bacteria that potentially can cause disease.

UseUse

Warnings

WARNINGS SECTION

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

WarningsWarnings

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds
  • Do not useDo not use

When using this product

OTC - WHEN USING SECTION

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

When usingWhen using

Stop use and ask a doctor

OTC - STOP USE SECTION

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

Stop useStop use

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.

Keep outKeep out

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.

DirectionsDirections

Other Information

STORAGE AND HANDLING SECTION

  • Storage and Handling-Store between 15-30C (59-86F),
  • Avoid freezing and excessive heat above 40C (104F)
  • Other informationOther information

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients-Water, Glycerin, Carbomer, Aminomethyl Propanol, Mentha Arvensis Leaf Oil, Tocopheryl Acetate, Panthenol, Sodium Hyaluronate, Aloe Barbadensis Leaf Extract

Inactive ingredientsInactive ingredients

Questions or Comments

OTC - QUESTIONS SECTION

Questions or Comments 1-800-819-4159

QuestionsQuestions

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EPU

INSTANT HAND SANITIZER

70% Ethyl Alcohol as recommended

Help Reduce Bacteria On The Skin.
For all day use

No Sticky

Deep Moisturizing

100 mL (3.38 fl. oz.)

Principal Display PanelPrincipal Display Panel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73862-201-212025-06-18C16284748780-1d6a99b39-f3fa-a426-e053-dadaa90af4c2EPU Hand Sanitizer 100ml
73862-201-212022-01-28C16284748780-1d6a99b39-f3fa-a426-e053-dadaa90af4c2EPU Hand Sanitizer 100ml

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73862-201HAND SANITIZER (ETHYLE ALCOHOL) GEL [E.CIS COSMETIC CO.,LTD]8Legacy NDC20200530_a212bf16-b6cc-050e-e053-2a95a90a9dd5.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73862-20173862-201-20, 73862-201-21

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
PANTHENOLWV9CM0O67ZIACT
HYALURONATE SODIUMYSE9PPT4THIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER 9404Q93RCW27EIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
MENTHA ARVENSIS LEAF OIL1AEY1M553NIACT

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
368d3bbc-ac2d-022a-e063-6294a90a1bb3a212bf16-b6cc-050e-e053-2a95a90a9dd52025-06-01WarningsExact identifier
spl set id: a212bf16-b6cc-050e-e053-2a95a90a9dd5

Reported adverse events (FAERS/openFDA)#

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