TOUGH GUY HAND SANITIZER WIPES TOUGH GUY- hand sanitizer wipes cloth

Tough Guy Hand Sanitizer Wipes by

Drug Labeling and Warnings

Tough Guy Hand Sanitizer Wipes by is a Otc medication manufactured, distributed, or labeled by W.W. Grainger, Inc., ITW Dymon. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient                                                                                                          Purpose

n-alkyl dimethyl benzyl ammonium chloride (0.1%)................................................Antiseptic

n-alkyl dimethyl ethyl benzyl ammonium chloride (0.1%)......................................Antiseptic

PURPOSE

Uses

• For hand washing to decrease bacteria on skin.
• Recommended for repeated use.
  

WHEN USING

Warnings

Flammable, keep away from heat and flame.

For external use only.

WHEN USING

When using this product

• do not get into eyes.  If contact occurs rinse eyes thoroughly with water.
  

STOP USE

Stop use and ask a doctor

• If irritation arises and persists for more than 72 hours.
  

KEEP OUT OF REACH OF CHILDREN

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

WHEN USING

Directions

• Wet hands thoroughly with product and allow to dry without wiping.
• Children under six years of age should be supervised when using this product.
  

QUESTIONS

Inactive Ingredients

Water, Ethanol, Mineral Oil, Isopropyl Myristate, C12-C14 Sec-pareth-5

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TOUGH GUY HAND SANITIZER WIPES  TOUGH GUY
hand sanitizer wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 40096-0802
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 970 mL
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.1 g  in 970 mL

Inactive Ingredients
Ingredient Name	Strength
Alcohol (UNII: 3K9958V90M)	20.0 g  in 970 mL
WATER (UNII: 059QF0KO0R)	78.1 g  in 970 mL
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)	0.3 g  in 970 mL
MINERAL OIL (UNII: T5L8T28FGP)	0.7 g  in 970 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 40096-0802-0	4 mL in 1 PACKET
2	NDC: 40096-0802-1	438 mL in 1 CONTAINER
3	NDC: 40096-0802-2	77 mL in 1 PACKAGE
4	NDC: 40096-0802-3	206 mL in 1 CONTAINER
5	NDC: 40096-0802-4	619 mL in 1 CONTAINER
6	NDC: 40096-0802-5	1134 mL in 1 CONTAINER
7	NDC: 40096-0802-6	1247 mL in 1 CONTAINER

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333	03/01/2010

Labeler - W.W. Grainger, Inc. (005103494)

Registrant - ITW Dymon (103307604)

Establishment
Name	Address	ID/FEI	Business Operations
ITW Dymon		103307604	manufacture