GENRX HAND SANITIZING- benzalkonium chloride spray

GenRx Hand Sanitizing by

Drug Labeling and Warnings

GenRx Hand Sanitizing by is a Otc medication manufactured, distributed, or labeled by PureTek Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Uses

■ a topical antiseptic that protects against germs

Warnings

For external use only

Do not use on

■ deep or puncture wounds ■ animal bites ■ serious burns

When using this product

■ do not get into eyes

Stop use and ask a doctor if

■ Irritation and redness develop
■ condition persists for more than 72 hours

Keep out of reach of children.

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

Directions

■ wet hands thoroughly with product
■ allow to dry without wiping
■ repeat as necessary

Other information

■ protect from freezing ■ avoid excessive heat

Inactive ingredients

Aloe barbadensis (Aloe vera) leaf juice, butylene glycol, disodium EDTA, glycerin, phenoxyethanol,

purified water, sodium hyaluronate.

GenRx Hand Sanitizing Spray (8 oz label)

INGREDIENTS AND APPEARANCE

GENRX HAND SANITIZING 
benzalkonium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59088-315
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
EDETATE DISODIUM (UNII: 7FLD91C86K)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59088-315-16	237 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/18/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/18/2020

Labeler - PureTek Corporation (785961046)