2XL MEGA ROLLS SANITIZING WIPES- benzalkonium chloride swab

2XL Mega Rolls Sanitizing Wipes by

Drug Labeling and Warnings

2XL Mega Rolls Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by 2xl Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium chloride 0.13%

Purpose

Antimicrobial

Uses

• to sanitize hands without requiring water or a rinse
• kills 99.9% of most common germs

Warnings

For external use only

When using this product

• do not use in or near the eye
• discontinue use if irritation and redness develop

Keep out of reach of children

In case of accidental ingestion, seek medical attention or contact a Poison Control Center immediately.

Directions

• wet hands thoroughly with wipe
• allow to dry without rinsing

Other information

Store at room temperature

Inactive ingredients

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

Questions? Comments?

Call (888)977-3726

Principal Display Panel

NDC: 71995-020-01

Kills 99.9% of most common germs that may cause illness

2XL Mega ROLL

2.3K

SANITIZING WIPES

2300 count megaroll

• Quickly removes soil and kills most common germs that may cause illness
• Textured for superior cleaning
• Sanitizes hand while cleaning effectively
• Convenient, easy to use and ideal for placement in offices, restaurants, health clubs, or anywhere else germs may be

NET CONTENTS 2300 Wipes per Roll (8'' X 5'')

Net Weight: 5460g/roll

INGREDIENTS AND APPEARANCE

2XL MEGA ROLLS SANITIZING WIPES 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71995-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 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: 71995-020-01	2300 in 1 BAG	01/02/2018
1		1 g in 1 PACKET; 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	03/16/2017

Labeler - 2xl Corporation (148004059)

Registrant - 2xl Corporation (148004059)