beCLEAN SANITIZING DEVICE WIPE

Manufacturer
World Amenities
Effective date
2020-07-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:21:57

Label at a glance#

ProductbeCLEAN SANITIZING DEVICE WIPE 75 PERCENT ALCOHOL
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

FOR HAND SANITIZING TO DECREASE BACTERIA ON THE SKIN. RECOMMENDED FOR REPEATED USE.

Dosage and administration

Apply enough product to cover hands thoroughly. Rub hands together, until hands feel dry. Do not rinse. Children under 6 years of age should be supervised when using this product. Not recommended for infants.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 75%

PURPOSE

OTC - PURPOSE SECTION

ANTISEPTIC

USES

INDICATIONS & USAGE SECTION

FOR HAND SANITIZING TO DECREASE BACTERIA ON THE SKIN. RECOMMENDED FOR REPEATED USE.

WARNINGS

WARNINGS SECTION

Flammable. Keep away from fire or flame.

Do not use in or near the eyes, in case of contact, rinse thoroughly with water.

For external use only. Stop use and ask a doctor if irritation or rash appears and lasts. Avoid contact with broken skin.

If swallowed, seek medical help immediately.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • Apply enough product to cover hands thoroughly.
  • Rub hands together, until hands feel dry. Do not rinse.
  • Children under 6 years of age should be supervised when using this product.
  • Not recommended for infants.

OTHER INFORMATION

OTHER SAFETY INFORMATION

Store below 105°F (40°C). May discolor some fabrics.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Aqua (Water)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_BeClean_Device_Sanitizing_Wipe_Rev_A_PDP01b LBL_BeClean_Device_Sanitizing_Wipe_Rev_A_PDP

01b LBL_BeClean_Device_Sanitizing_Wipe_Rev_A_DF Box01b LBL_BeClean_Device_Sanitizing_Wipe_Rev_A_DF Box

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53950-1005-12021-07-23C16284748780-1c7ccaba7-14d9-fd44-e053-dadaa90aa01bbeCLEAN SANITIZING DEVICE WIPE 75% ALCOHOL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53950-1005-1beCLEAN SANITIZING DEVICE WIPE75 PERCENT ALCOHOL1 in 1 POUCHSOLUTION11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53950-1005BECLEAN SANITIZING DEVICE WIPE 75 PERCENT ALCOHOL (ALCOHOL) SOLUTION [WORLD AMENITIES]1Legacy NDC, 1 package rows20200720_d3696e56-7515-4165-b053-9e78b57371bd.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53950-100553950-1005-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
27c87d97-d144-4723-ab45-af184156b4edd3696e56-7515-4165-b053-9e78b57371bd2020-07-19WarningsExact identifier
spl id: 27c87d97-d144-4723-ab45-af184156b4ed
spl set id: d3696e56-7515-4165-b053-9e78b57371bd

Reported adverse events (FAERS/openFDA)#

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