BENZA CLEAN HAND SANITIZER- benzalkonium chloride liquid

Benza Clean hand sanitizer by

Drug Labeling and Warnings

Benza Clean hand sanitizer by is a Otc medication manufactured, distributed, or labeled by BIOSYN INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13% 

Purpose

Antimicrobial and First Aid Antiseptic

Uses

For hand sanitizing to decrease bacteria on the skin. As a wound antiseptic to help prevent bacterial contamination in cuts, burns, scrapes, lacerations and skin infections.

Warnings

For external use only.

WHEN USING

When using this product avoid contact with eyes. Incase of eye contact, flush eyes with water.
Discontinue useif irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Pump onto hands as needed. Rub briskly until dry.
• Apply to wounds 3 times per day after cleaning. Allow to dry. May be bandaged once dry.

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Water, Sodium Bicarbonate, Colalipid C, Hydroxyethyl Cellulose, Green Tea Leaf Extract.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

BENZA CLEAN HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79832-001
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
WATER (UNII: 059QF0KO0R)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79832-001-01	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/18/2020
2	NDC: 79832-001-02	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/18/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/18/2020

Labeler - BIOSYN INC (079797906)