TC ALCOHOL-FREE HAND SANITIZER- benzethonium chloride liquid

TC Alcohol-Free Hand Sanitizer by

Drug Labeling and Warnings

TC Alcohol-Free 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]

SPL UNCLASSIFIED SECTION

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.

• READ MATERIAL SAFETY DATA SHEET BEFORE USING PRODUCT.

Directions

Apply generously to hands. Rub hands together. Allow hands to dry. Repeat daily as necessary.

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 - 800 mL Pouch Box

Rubbermaid®
Commercial Products
TECHNICAL CONCEPTS

Alcohol-Free Hand Sanitizer

800 mL (27 FL. OZ. U.S.)

INGREDIENTS AND APPEARANCE

TC ALCOHOL-FREE HAND SANITIZER 
benzethonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65321-034
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)
PEG-6 Caprylic/Capric Glycerides (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: 65321-034-01	4 in 1 BOX	10/28/2019
1		800 mL in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 65321-034-02	4 in 1 BOX	10/28/2019
2		1100 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(65321-034) , RELABEL(65321-034) , REPACK(65321-034) , MANUFACTURE(65321-034)