WIPE N GO- benzalkonium chloride swab

Drug Labeling and Warnings

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride, 0.1%

Purpose

Antibacterial

Uses

Antibacterial wipes for the skin.

Warnings

For external use only.

Do not use

over large areas of the body if you are allergic to any of the ingredients.

When using this product

do not 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 24 hours.

Keep out of reach of children

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

Directions:

For adults and children of 2 years and over, use on hands and face to clean and refresh, allow skin to air dry.

For children under 2 years, ask a doctor before use.

SPL UNCLASSIFIED SECTION

Inactive ingredients:

Water, Disodium EDTA, Phenoxyethanol, Glycine, Polysorbate 20, Glycerin, Fragrance, Polyaminopropyl Biguanide, Sodium Citrate

Principal Display Panel

wipe n' go

Antibacterial HAND WIPES

Made in China

Distributed by: Canadia USA Corporation.

INGREDIENTS AND APPEARANCE

WIPE N GO 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69538-200
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
GLYCINE (UNII: TE7660XO1C)
WATER (UNII: 059QF0KO0R)
EDETATE DISODIUM (UNII: 7FLD91C86K)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
GLYCERIN (UNII: PDC6A3C0OX)
POLIHEXANIDE (UNII: 322U039GMF)
SODIUM CITRATE (UNII: 1Q73Q2JULR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69538-200-01	24 in 1 BOX
1		10 in 1 PACKAGE
1		3 g in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 69538-200-02	4 in 1 BOX
2		10 in 1 CARTON
2		10 in 1 PACKAGE
2		3 g in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 69538-200-03	8 in 1 BOX
3		10 in 1 CARTON
3		10 in 1 PACKAGE
3		3 g in 1 PACKET; Type 0: Not a Combination Product
4	NDC: 69538-200-04	12 in 1 BOX
4		10 in 1 CARTON
4		10 in 1 PACKAGE
4		3 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	08/24/2015

Labeler - CANADIA USA CORPORATION (012119600)

Establishment
Name	Address	ID/FEI	Business Operations
Nox-Bellcow (Zhongshan) Nonwo ven Chemical Ltd		528103343	manufacture(69538-200)