TC ENRICHED FOAM ALCOHOL-FREE PLUS HAND SANITIZER- benzethonium chloride liquid

TC Enriched Foam Alcohol-Free Plus Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

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Drug Facts

Active Ingredient

0.1% Benzethonium Chloride

Purpose

Antiseptic

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

Wet hands thoroughly with product and allow to dry without wiping.

Inactive Ingredients

Water (Aqua), Propylene Glycol, PEG-6 Caprylic/Capric Glycerides, Phenoxyethanol, Decylamine Oxide, Tetrasodium Glutamate Diacetate, Sodium Hydroxide, Caprylyl Glycol, Ethylhexylglycerin, Lactic Acid, Disodium Lauriminodipropionate Tocopheryl Phosphates, Benzoic Acid, Dehydroacetic Acid, Shea Butteramidopropyl Betaine, Hexylene Glycol, 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 - 1300 mL Pouch Label

Rubbermaid®
Commercial Products

TECHNICAL CONCEPTS

NSF®

Nonfood Compounds
Program Listed E3
NSF Registration #143589

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

1300 mL (44 FL. OZ. U.S.)

© 2017 | 2049955 FRONT V-10-2017

PRFR13007 V-10-2017 FRONT

INGREDIENTS AND APPEARANCE

TC ENRICHED FOAM ALCOHOL-FREE PLUS HAND SANITIZER 
benzethonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65321-035
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzethonium Chloride (UNII: PH41D05744) (Benzethonium - UNII:1VU15B70BP)	Benzethonium Chloride	0.1 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)
Disodium Lauriminodipropionate Tocopheryl Phosphates (UNII: 0K5Y9U1P6M)
Benzoic Acid (UNII: 8SKN0B0MIM)
Dehydroacetic Acid (UNII: 2KAG279R6R)
Hexylene Glycol (UNII: KEH0A3F75J)
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65321-035-01	3 in 1 BOX	10/28/2019
1		1300 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 not final	part333A	10/28/2019

Labeler - Rubbermaid Commercial Products LLC (049924368)

Establishment
Name	Address	ID/FEI	Business Operations
NWL Netherlands Production BV		489421698	ANALYSIS(65321-035) , RELABEL(65321-035) , REPACK(65321-035) , MANUFACTURE(65321-035)