FDA.reportPublic FDA data

BEIS Advanced Hand Sanitizer

Manufacturer
Beis LLC
Effective date
2021-11-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:45:05

Label at a glance#

ProductBEIS Advanced Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

For hand washing to help reduce bacteria that potentially can cuase disease. Recommended for repeated use. For use when soap and water are not available.

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Children under 6 years of age should be supervised by adult when applying this product. Do not use on children less than 2 months of age or on open skin wounds.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • For hand washing to help reduce bacteria that potentially can cuase disease. Recommended for repeated use. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only

Flammable, Keep away from heat or flame

When using this product

OTC - WHEN USING SECTION

do not use in or near 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

if irritation or rash appears on the skin.

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.
  • Children under 6 years of age should be supervised by adult when applying this product.
  • Do not use on children less than 2 months of age or on open skin wounds.

Other information

SPL UNCLASSIFIED SECTION

  • Store between 15-30°C (59-86°F)
  • Avoid freezing and excessive heat above 40°C (104°F)
  • May discolor some fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Squalane, Panthenol, Inulin, Sodium Hyaluronate, Fructose, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

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
81263-001-012024-01-30C16284748780-11030e365-5519-111a-e063-dadaa90a10e2BEIS Advanced Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81263-001-01BEIS Advanced Hand Sanitizer4 in 1 PACKAGEGEL42
81263-001-01BEIS Advanced Hand Sanitizer60 mL in 1 BOTTLEGEL602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81263-001BEIS ADVANCED HAND SANITIZER (ALCOHOL) GEL [BEIS LLC]2Legacy NDC, 2 package rows20211124_c093cb85-c78e-b3aa-e053-2995a90af54e.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
81263-00181263-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
SQUALANEGW89575KF9IACT
PANTHENOLWV9CM0O67ZIACT
INULINJOS53KRJ01IACT
HYALURONATE SODIUMYSE9PPT4THIACT
FRUCTOSE6YSS42VSEVIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
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
d178ee5f-236d-2bce-e053-2a95a90add02c093cb85-c78e-b3aa-e053-2995a90af54e2021-11-23WarningsExact identifier
spl id: d178ee5f-236d-2bce-e053-2a95a90add02
spl set id: c093cb85-c78e-b3aa-e053-2995a90af54e

Reported adverse events (FAERS/openFDA)#

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