LAURA GELLER ANTIBACTERIAL HAND SANITIZING WIPES- benzalkonium chloride cloth

LAURA GELLER antibacterial hand sanitizing wipes by

Drug Labeling and Warnings

LAURA GELLER antibacterial hand sanitizing wipes by is a Otc medication manufactured, distributed, or labeled by Hangzhou Glamcos Biotech CO.,LTD, Hangzhou Glamcos Biotech CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.2%

Purpose

Antibacterial

Use

For hand sanitization and decreasing amount of bacteria on skin.

Warnings

For External Use Only.
Do Not Use on children less than 2 years of age.
On open wounds/cuts.
When Using This Product keep out of eyes,ears and mouth.In case of contact with eyes,rinse thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs.These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed,get medical help or contact the poison control center immediately.

Directions

Rub cloth between hands for complete cleansing and let hands air dry.
Children under 6 years of age should be supervised when using.

Inactive Ingredients

Water, Phenoxyethanol, Didecylmdimonium Chloride, Propylene Glycol, Chlophenesin

Package Label

INGREDIENTS AND APPEARANCE

LAURA GELLER ANTIBACTERIAL HAND SANITIZING WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76635-220
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CHLORPHENESIN (UNII: I670DAL4SZ)
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Product Characteristics
Color		Score
Shape	SQUARE (20 Piece Cloth)	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76635-220-20	105 g in 1 BAG; Type 0: Not a Combination Product	08/11/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	08/11/2020

Labeler - Hangzhou Glamcos Biotech CO.,LTD (554476017)

Registrant - Hangzhou Glamcos Biotech CO.,LTD (554476017)

Establishment
Name	Address	ID/FEI	Business Operations
Hangzhou Glamcos Biotech CO., LTD		554476017	manufacture(76635-220)