BOOGIE HANDS ANTIBACTERIAL WET WIPES (benzalkonium chloride- 0.115% cloth

Boogie Hands Antibacterial Wet Wipes by

Drug Labeling and Warnings

Boogie Hands Antibacterial Wet Wipes by is a Otc medication manufactured, distributed, or labeled by ELEEO BRANDS LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Benalkonium chloride (0.115%)

Purpose

Antibacterial

Use

For hand sanitizing to decrease bacteria on skin

Warnings

For external use only

Do Not Use

if you are allergic to any of the ingredients

When using this product

donot get into eyes.

if contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

irritation or rash develops.

and continues for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away

Directions:

*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

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

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BOOGIE HANDS ANTIBACTERIAL WET WIPES 
benzalkonium chloride (0.115%) cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79747-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.0012 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SORBITOL (UNII: 506T60A25R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
EDETATE SODIUM (UNII: MP1J8420LU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79747-005-20	3 in 1 CARTON	07/22/2020
1		20 mL in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 79747-005-02	20 mL in 1 PACKAGE; Type 0: Not a Combination Product	07/22/2020
3	NDC: 79747-005-30	1 in 1 CARTON	07/22/2020
3		30 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/22/2020

Labeler - ELEEO BRANDS LLC (078476782)