Boogie Hands Antibacterial Wet Wipes

Manufacturer
ELEEO BRANDS LLC
Effective date
2025-09-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:42:13

Label at a glance#

ProductBoogie Hands Antibacterial Wet Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Dosage and administration

Rub wipe over all surfaces of both hands. Wet hands thoroughly with wipe. Allow to dry without wiping. Children under 2 years of age:ask doctor prior to use. Children under 6 years of age:use adult supervision.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Benalkonium chloride (0.13%)

Purpose

OTC - PURPOSE SECTION

Antimicrobial

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

avoid contact with the eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

if irritation or redness develops.

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

  • Rub wipe over all surfaces of both hands. Wet hands thoroughly with wipe.
  • Allow to dry without wiping.
  • Children under 2 years of age:ask doctor prior to use.
  • Children under 6 years of age:use adult supervision.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water, Decyl glucoside, Aloe barbadensis(aloe) leaf extract, Tocopheryl (Vitamin E) acetate, Disodium EDTA, Potassium sorbate, Sodium benzoate, Phenoxyethanol, Citric acid, Fragrance

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

20ct NDC:79747-014-02 20ct NDC: 79747-014-0220ct NDC: 79747-014-02

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130816167012219GTIN-13: 0816167012219
EAN-13: 0816167012219
GTIN-12: 816167012219
UPC-A: 816167012219
GTIN storage (14 digits): 00816167012219
6003E Boogie Hands Pack PROOF6.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79747-014-02Boogie Hands Antibacterial Wet Wipes20 mL in 1 PACKETCLOTH201
79747-014-20Boogie Hands Antibacterial Wet Wipes20 mL in 1 POUCHCLOTH201
79747-014-20Boogie Hands Antibacterial Wet Wipes3 in 1 CARTONCLOTH31
79747-014-30Boogie Hands Antibacterial Wet Wipes1 in 1 CARTONCLOTH11
79747-014-30Boogie Hands Antibacterial Wet Wipes30 mL in 1 PACKETCLOTH301
79747-014-40Boogie Hands Antibacterial Wet Wipes2 in 1 CARTONCLOTH21
79747-014-40Boogie Hands Antibacterial Wet Wipes20 mL in 1 PACKETCLOTH201
79747-014-80Boogie Hands Antibacterial Wet Wipes4 in 1 CARTONCLOTH41
79747-014-80Boogie Hands Antibacterial Wet Wipes20 mL in 1 POUCHCLOTH201

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79747-01479747-014-20, 79747-014-02, 79747-014-30, 79747-014-40, 79747-014-80

Ingredients#

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

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

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
Boogie Hands Antibacterial Wet WipesBENZALKONIUM CHLORIDE (0.13%)ELEEO BRANDS LLC4009eb93-cef6-a202-e063-6394a90ae61b2025-09-30WarningsExact identifier
ndc (package): 79747-014-02
ndc (package): 79747-014-80
ndc (package): 79747-014-30
ndc (package): 79747-014-40
ndc (package): 79747-014-20
ndc (product): 79747-014
ndc11 (package): 79747001402
ndc11 (package): 79747001480
ndc11 (package): 79747001430
ndc11 (package): 79747001420
ndc11 (package): 79747001440
spl id: 4009ebb1-142a-64a8-e063-6294a90a7555
spl set id: 4009eb93-cef6-a202-e063-6394a90ae61b

Reported adverse events (FAERS/openFDA)#

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