Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Use

to decrease bacteria on the skin

Warnings

for external use only: hands only

When using this product

avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
avoid contact with broken skin

Stop use and ask a doctor if

if irritation and redness develop
condition persists for more than 72 hours

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center right away

Directions

wet hands thoroughly with product and allow to dry without wiping
for children under 6, use only under adult supervision
not recommended for infants

Inactive ingredients

cetrimonium chloride, diglycerin, disodium cocoamphodiacetate, fragrance, glycerin, hydrochloric acid, methoxy PEG/PPG-7/3 aminopropyl dimethicone, sodium benzoate, tetrasodium EDTA, water

Rear label text

Distributed by

Veritiv Operating Company

Atlanta, GA 30328

reliablebrand.com

PRINCIPAL DISPLAY PANEL

ALCOHOL FREE FOAM HAND SANITIZER

Manual push style

1 L (33.8 FL OZ)

image description

FOAMING HAND SANITIZER
benzalkonium chloride lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71897-118
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
DIGLYCERIN (UNII: 3YC120743U)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROCHLORIC ACID (UNII: QTT17582CB)
METHOXY PEG/PPG-7/3 AMINOPROPYL DIMETHICONE (UNII: 4M7P1JZ2V2)
SODIUM BENZOATE (UNII: OJ245FE5EU)
EDETATE SODIUM (UNII: MP1J8420LU)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:71897-118-45	1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/05/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/05/2020

Labeler - VERITIV OPERATING COMPANY (006989982)

Registrant - Vi-Jon, LLC (790752542)

Name	Address	ID/FEI	Business Operations
Establishment
Vi-Jon, LLC		790752542	manufacture(71897-118)

Name	Address	ID/FEI	Business Operations
Establishment
Vi-Jon, LLC		088520668	manufacture(71897-118)

Foaming Hand Sanitizer 118.401/118AE