ENRICHED FOAM ALCOHOL-FREE HAND SANITIZER- benzalkonium chloride liquid

Enriched Foam Alcohol-Free Hand Sanitizer by

Drug Labeling and Warnings

Enriched Foam Alcohol-Free Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Rubbermaid Commercial Products LLC, NWL Netherlands Services B.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active Ingredient

0.13% Benzalkonium Chloride

Purpose

Antiseptic Cleaner

Use

To decrease potentially harmful germs on skin.

Warnings

• For external use only.

• When using this product avoid contact with eyes. In case of eye contact, flush with water.

• Stop use and ask a doctor, if irritation or redness persist.

• Do not ingest.

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

Directions

Place hands under the dispenser, allow 0.4 mL of foam into hands, rub thoroughly over the surface of both hands for at least 30 seconds, and then allow hands dry

Inactive Ingredients

Water (Aqua), Propylene Glycol, PEG-6 Caprylic/Capric Glycerides, Phenoxyethanol, Decylamine Oxide, Tetrasodium Glutamate Diacetate, Sodium Hydroxide, Caprylyl Glycol, Ethylhexylglycerin, Lactic Acid, Shea Butteramidopropyl Betaine, Sodium Chloride, Hexylene Glycol, Benzoic Acid, Tocopherol, Sodium Citrate

Questions?

1-800-347-9800 Mon – Fri, 8 AM – 5 PM EST

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Distributed by | Rubbermaid Commercial Products LLC
3124 Valley Avenue, Winchester, VA U.S.A. 22601-2694

PRINCIPAL DISPLAY PANEL - 1100 mL Pouch Label

Rubbermaid®
Commercial Products

Enriched Foam Alcohol-Free Hand Sanitizer
With Shea Butter & Vitamin E

NSF®

Nonfood Compounds
Program Listed E3
NSF Registration #143589

1100 mL (37.2 FL. OZ. U.S.)

© 2021 | 2147031 | PRFR11080 FRONT
PRFR11080 V-06-2021 FRONT

INGREDIENTS AND APPEARANCE

ENRICHED FOAM ALCOHOL-FREE HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65321-039
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	13 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CAPRYLOCAPROYL POLYOXYLGLYCERIDES 6 (UNII: GO50W2HWO8)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DECYLAMINE OXIDE (UNII: G387VUT5EZ)
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
BENZOIC ACID (UNII: 8SKN0B0MIM)
.ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9)
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65321-039-01	4 in 1 BOX	06/21/2021
1		1100 mL in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 65321-039-02	4 in 1 BOX	06/21/2021
2		1300 mL in 1 POUCH; Type 0: Not a Combination Product
3	NDC: 65321-039-03	6 in 1 BOX	06/21/2021
3		800 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH DRUG	M004	06/21/2021

Labeler - Rubbermaid Commercial Products LLC (049924368)

Establishment
Name	Address	ID/FEI	Business Operations
NWL Netherlands Services B.V.		494692088	ANALYSIS(65321-039) , MANUFACTURE(65321-039)