ANTIBACTERIAL WET WIPES- benzalkonium chloride swab

Antibacterial Wet Wipes by

Drug Labeling and Warnings

Antibacterial Wet Wipes by is a Otc medication manufactured, distributed, or labeled by MC Group Development Ltd. , MC Group Development Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride

Purpose

Antibacterial

Use

For hand washing to decrease bacteria on the skin.May be used on face,arms and legs.

WARNINGS

For External use only.
Keep out of eyes,Incase of contact,rinse with water.If irritation or rash develops,discontinue use .Consult doctor if irritation persists for more than 72 hours,If swallowed,seek medical attention or contact a Poison Control Center.

keep out of reach of children

keep out of reach of children

Directions

Open resealable label.Pull one sheet from pack.Clean hands or affected area and discard.Re-seal label after each use to keep wipes fresh.

Inactive ingredients

Iodopropynyl Butylcarbamate,DMDM Hydantoin,Lauryl Glucoside,Glycerin,D-Panthenol,Tocopheryl Acetate,Chamomilla Recutita Extract,PEG-12 Dimethicone,Disodium EDTA,Aloe Barbadensis Leaf Extract,Allantoin,Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL WET WIPES 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50672-838
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	Benzalkonium Chloride	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
Iodopropynyl Butylcarbamate (UNII: 603P14DHEB)
DMDM Hydantoin (UNII: BYR0546TOW)
Lauryl Glucoside (UNII: 76LN7P7UCU)
GLYCERIN (UNII: PDC6A3C0OX)
DEXPANTHENOL (UNII: 1O6C93RI7Z)
TOCOPHERYL NICOTINATE, D-.ALPHA. (UNII: WI1J5UCY5C)
MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
Allantoin (UNII: 344S277G0Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50672-838-01	3.3 g in 1 POUCH

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/12/2012

Labeler - MC Group Development Ltd. (527868588)

Establishment
Name	Address	ID/FEI	Business Operations
MC Group Development Ltd.		527868588	manufacture(50672-838)