SCRUBS FOAMING HAND SANITIZER SCRUBS- hand sanitizer foam solution

SCRUBS Foaming Hand Sanitizer by

Drug Labeling and Warnings

SCRUBS Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by ITW Dymon. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PRINCIPAL DISPLAY PANEL

ACTIVE INGREDIENT

Active Ingredients                                                                                           Purpose

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

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

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

When using this product

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

PURPOSE

Uses

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

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.
  

WHEN USING

Warnings
Flammable, keep away from heat and flame.
For external use only.

QUESTIONS

Inactive Ingredients
Water, ethanol, Mineral Oil, Isoproply Myristate, C12-C14 Sec-pareth-5

INGREDIENTS AND APPEARANCE

SCRUBS FOAMING HAND SANITIZER  SCRUBS
hand sanitizer foam solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51239-1929
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 g  in 970 mL
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 970 mL

Inactive Ingredients
Ingredient Name	Strength
Mineral Oil (UNII: T5L8T28FGP)	0.7 g  in 970 mL
Isopropyl Myristate (UNII: 0RE8K4LNJS)	0.3 g  in 970 mL
Alcohol (UNII: 3K9958V90M)	20 g  in 970 mL
Water (UNII: 059QF0KO0R)	78.02 g  in 970 mL

Product Characteristics
Color		Score
Shape		Size
Flavor	LEMON	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51239-1929-7	252 mL in 1 BOTTLE, PUMP

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333	10/01/2009

Labeler - ITW Dymon (103307604)

Registrant - ITW Dymon (103307604)

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