QUALITY CHOICE ANTIBACTERIAL MOIST TOWELETTES- benzalkonium chloride cloth

QUALITY CHOICE Antibacterial Moist Towelettes by

Drug Labeling and Warnings

QUALITY CHOICE Antibacterial Moist Towelettes by is a Otc medication manufactured, distributed, or labeled by Chain Drug Marketing Association. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.10%

Purpose

Antimicrobial

Uses

For hand sanitizing to decrease bacteria on skin.
Recommended for repeated use.

Warnings

For external use only

When using this product

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

Stop use and ask a doctor

if irritation or redness develpos, or if condition persists for more than 72 hours.

Keep out of reach of children.

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

Directions

Open cap, remove one wipe and unfold.
Wet hands throughly with product and allow to air dry.

Other Information

Store below 95 F(35C)  Keep Cap-Closed Tightly
May discolor certain fabrics or surfaces.

Inactive ingredients

Water, SD Alcohol 40, Phenoxyethanol, Decyl Glucoside, Potassium Sorbate, Sodium Benzoate, Disodium EDTA, Citric Acid, Aloe Barbadensis (Aloe) Leaf Extract, Fragrance

Principal Display Panel

Compare to Wet Ones**
QC
QUALITY
CHOICE
KILLS 99.9%
OF GERMS*
Fresh Scent
Antibacterial
Moist Towelettes
Moisturizing Formula
40
THICK MOIST CLOTHS
7 IN X 5.75 IN
(17.8 cm x 14.6 cm)
*Kills 99.9 %of germs that may cause illness including E Coli and MRSA in just 15 seconds

INGREDIENTS AND APPEARANCE

QUALITY CHOICE ANTIBACTERIAL MOIST TOWELETTES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63868-100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.10 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
EDETATE DISODIUM (UNII: 7FLD91C86K)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63868-100-40	40 in 1 CANISTER

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/03/2013

Labeler - Chain Drug Marketing Association (011920774)