BENZOCLEAN HAND SANITIZER- benzalkonium chloride gel

BENZOCLEAN HAND SANITIZER by

Drug Labeling and Warnings

BENZOCLEAN HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by GADAL Laboratories, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

ACTIVE INGREDIENT

Active Ingredient

Benzalkonium Chloride 0.13%

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Use ▪ For handwashing to decrease bacteria on the skin.

WARNINGS

Warnings For external use only. Do not use ▪ in the eyes Stop use and ask a doctor if ▪ irritation and redness develop ▪ if condition persists for more than 72 hours.

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

DOSAGE & ADMINISTRATION

Directions ▪ Place enough product in your palm to thoroughly cover your hands. ▪ Rub hands together briskly until dry. ▪ No rinsing required. No towels needed.

STORAGE AND HANDLING

Other information Store at room temperature.

INACTIVE INGREDIENT

Inactive ingredients Water (Aqua), Aloe Barbadensis Leaf Juice, Disodium EDTA, DMDM Hydantoin, Fragrance, Glycerin, Hydroxyethylcellulose, Sodium Chloride, Tocopheryl Acetate.

SPL UNCLASSIFIED SECTION

ADVANCED

MOISTURIZING 

LONG-LASTING GEL

WITH ALOE VERA & VITAMIN E

KILLS 99.9% OF GERMS

*Kills Most Viruses

*Moisturizes & Leaves

Hands Feeling Smooth

MADE IN THE USA

GMP GOOD MANUFACTURING PRACTICE QUALITY PRODUCT 

Distributed by: PCO Foods  1110 Powers Place Alpharetta, GA, 30009  pcofoods.com Questions or comments: sales@pcofoods.com

Packaging

INGREDIENTS AND APPEARANCE

BENZOCLEAN HAND SANITIZER 
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53113-090
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 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
DMDM HYDANTOIN (UNII: BYR0546TOW)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53113-090-08	236.5 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/01/2020

Labeler - GADAL Laboratories, Inc (841305639)

Establishment
Name	Address	ID/FEI	Business Operations
GADAL Laboratories, Inc		841305639	manufacture(53113-090)