FDA.reportPublic FDA data

Boogie Hands Antibacterial Wet Wipes

Manufacturer
ELEEO BRANDS LLC
Effective date
2022-12-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:52:22

Label at a glance#

ProductBoogie Hands Antibacterial Wet Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

*adults and children 2 years and over apply to hands  allow to dry without wiping *children under 2 years ask a doctor before use 

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Benalkonium chloride (0.115%)

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on skin

Warnings

WARNINGS SECTION

For external use only

Do Not Use

OTC - DO NOT USE SECTION

if you are allergic to any of the ingredients

When using this product

OTC - WHEN USING SECTION

donot get into eyes.

if contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash develops.

and continues for more than 72 hours

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

*adults and children 2 years and over

  • apply to hands 
  • allow to dry without wiping

*children under 2 years

  • ask a doctor before use 

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Gycerin, Fragrance, Aloe extract, Disodium EDTA , Propylene Glycol, Sorbitol

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

22

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049374benzalkonium Cl 0.115 % Medicated PadPSN2
1049374benzalkonium chloride 1.15 MG/ML Medicated PadSCD2
1049374benzalkonium chloride 0.115 % Medicated PadSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79747-005-022024-01-30C16284748780-11030e365-43c7-111a-e063-dadaa90a10e2Boogie Hands Antibacterial Hand Wipes
79747-005-202024-01-30C16284748780-11030e365-43c7-111a-e063-dadaa90a10e2Boogie Hands Antibacterial Hand Wipes
79747-005-302024-01-30C16284748780-11030e365-43c7-111a-e063-dadaa90a10e2Boogie Hands Antibacterial Hand Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79747-005-02Boogie Hands Antibacterial Wet Wipes20 mL in 1 PACKAGECLOTH202
79747-005-20Boogie Hands Antibacterial Wet Wipes3 in 1 CARTONCLOTH32
79747-005-20Boogie Hands Antibacterial Wet Wipes20 mL in 1 POUCHCLOTH202
79747-005-30Boogie Hands Antibacterial Wet Wipes1 in 1 CARTONCLOTH12
79747-005-30Boogie Hands Antibacterial Wet Wipes30 mL in 1 POUCHCLOTH302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79747-005BOOGIE HANDS ANTIBACTERIAL WET WIPES (BENZALKONIUM CHLORIDE (0.115%)) CLOTH [ELEEO BRANDS LLC]2Legacy NDC, 5 package rows20221209_ee68ba3b-a8f6-0f06-e053-2a95a90a7a19.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
79747-00579747-005-20, 79747-005-02, 79747-005-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SORBITOL506T60A25RIACT
ALOE VERA LEAFZY81Z83H0XIACT
EDETATE SODIUMMP1J8420LUIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
ef4656ac-6cf4-b316-e053-2995a90a37a1ee68ba3b-a8f6-0f06-e053-2a95a90a7a192022-12-07WarningsExact identifier
spl id: ef4656ac-6cf4-b316-e053-2995a90a37a1
spl set id: ee68ba3b-a8f6-0f06-e053-2a95a90a7a19

Reported adverse events (FAERS/openFDA)#

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