HAND SANITIZER- benzalkonium chloride solution

HAND SANITIZER by

Drug Labeling and Warnings

HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by QBLUE TECHNOLOGIES, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts - Active Ingredient

Benzalkonium Chloride 0.09%

Purpose

Antiseptic

Uses

Hand sanitizer to help reduce bacteria that potentially can cause disease.

Warnings

For external use only.

When using this product

Keep out of eyes. In case of contact with eyes, rinse eye thoroughly with water.

Do not Use

on open skin wounds.

Stop Use and ask a doctor

if irritation or rash occurs.

Keep out of reach of children.

If swallowed, get medical help or contact poison control center right away.

Directions

• Spray onto hands or skin and apply evenly until dry.
• Do not dilute. Use as directed.

Other Information

• Store at room temperature. Avoid direct sunlight.
• Do not refrigerate.
• Use within 9 months after opening

Inactive Ingredients

titanium dioxide, purified water

Questions or comment?

1-833-387-9949

PDP

NDC: 83388-001-15

Alcohol-free non-allergenic water-based sanitizing solution. Kills and blocks 99.9% of all germs. Made without parabens, sulfates, phthalates, fragrances or dyes. Gentle and safe for children, pets, elders, and the environment.

Science-based
Pure Ingredients
Net WT: 5 fl.oz (150 mL)
Reuse and
recycle
Made in Hong Kong, China.
US patent no. 17049546
Distributed By
QBlue Technologies, Inc.
4521 PGA Blvd STE 510
Palm Bch Gardens, FL 33418

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83388-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.9 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83388-001-15	150 mL in 1 POUCH; Type 0: Not a Combination Product	04/10/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/10/2023

Labeler - QBLUE TECHNOLOGIES, INC. (118928041)