FDA.reportPublic FDA data

PLUSBEAU VISAGE Hand Sanitizing Gel 62% 250ml

Manufacturer
Visage Cosmetic Co., Ltd | E.CIS Cosmetic Co.,Ltd
Effective date
2020-05-25
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:17:24

Label at a glance#

ProductPLUSBEAU VISAGE Hand Sanitizing Gel 62% 250ml
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

Ethyl Alcohol 62% v/v. Purpose: Antiseptic

62 Alcohol Gel 250ml62 Alcohol Gel 250ml

Purpose

OTC - PURPOSE SECTION

Antiseptic

62 Alcohol Gel 25062 Alcohol Gel 250

Use

INDICATIONS & USAGE SECTION

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

62 Alcohol Gel62 Alcohol Gel

Warnings

WARNINGS SECTION

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

WarningWarning

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

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

keep out of reach of childrenkeep out of reach of children

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.

directiondirection

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, Carbomer, Aminomethyl Propanol, Mentha Arvensis Leaf Oil, Tocopheryl Acetate, Panthenol, Sodium Hyaluronate, Aloe Barbadensis Leaf Extract

inactive ingredientsinactive ingredients

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PLUSBEAU VISAGE Hand Sanitizing Gel
Aloe Barbadensis Leaf Extract
Cleanliness & Moisturizing
Easy to use!
Hand Sanitizing & Moisturizing
Help Reduce Bacteria on the skin
250 mL / 8.45 fl. oz.

PDPPDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN3
581660ethanol 0.62 ML/ML Topical GelSCD3
581660ethanol 62 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74441-101-022022-01-28C16284748780-1d6a99b39-f560-a426-e053-dadaa90af4c2PLUS BEAU VISAGE Hand Sanitizing Gel 62% 250ml

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74441-101-01PLUSBEAU VISAGE Hand Sanitizing Gel 62% 250ml250 mL in 1 BOTTLELIQUID2503
74441-101-02PLUSBEAU VISAGE Hand Sanitizing Gel 62% 250ml30 in 1 CASELIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74441-101PLUSBEAU VISAGE HAND SANITIZING GEL 62% 250ML (ETHYL ALCOHOL) LIQUID [VISAGE COSMETIC CO., LTD]3Legacy NDC, 2 package rows20200613_a2afa303-1ee3-ff97-e053-2a95a90afe55.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
74441-10174441-101-01, 74441-101-02

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
MENTHA ARVENSIS LEAF OIL1AEY1M553NIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
PANTHENOLWV9CM0O67ZIACT
ALCOHOL3K9958V90MACTIB
AMINOMETHYLPROPANOLLU49E6626QIACT
HYALURONATE SODIUMYSE9PPT4THIACT
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER 9404Q93RCW27EIACT

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
a6727709-58a9-526c-e053-2a95a90a5d81a2afa303-1ee3-ff97-e053-2a95a90afe552020-05-25WarningsExact identifier
spl id: a6727709-58a9-526c-e053-2a95a90a5d81
spl set id: a2afa303-1ee3-ff97-e053-2a95a90afe55

Reported adverse events (FAERS/openFDA)#

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