SANITIZE AWAY- isopropyl alcohol gel

Sanitize Away by

Drug Labeling and Warnings

Sanitize Away by is a Otc medication manufactured, distributed, or labeled by Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Isopropyl Alcohol....72%

Purpose

Antimicrobial

Uses

• For hand sanitizing to decrease bacteria on the skin

Warnings

• For external use only.
• Flammable keep away from fire or flame

When using this product

• Avoid contact with eyes. In case of eye contract, flush eyes with water. 

Stop use and ask doctor if

• irritation or redness develops, if condition persists for more than 72 hours.  

Keep out of reach of children

If swallowed, get medical help or contact a Poison Conrol Center right away

Directions

• Place a small amount of Sanitize Away in your palm to throughly cover your hands. 
• Rub hands together briskly until dry. 
• For children under 6 years of age should be supervised when using this product. 

Inactive Ingredients

• Water
• Glycerin
• Propylene Glycol

Sanitize Away

72% Alcohol Hand Sanitizer, Category E3

• 72% Isopropyl Alcohol
• Contains Emollients to Soothe the Skin
• Quick Drying

Sanitize Away is an E3-rated, no-rinse hand sanitizer.Contain emollient to moisture and sooth the skin.Specially formulated to be fragrance-free, dye-free, and acceptable for use in sensitive environments like: Hospitals, Food Processors, and other Food Service Establishments.

Sanitize Away contains at least 72% of Isopropyl Alcohol and meets Center Disease Control guidelines for hand hygiene in healthcare settings.

1 gallon

INGREDIENTS AND APPEARANCE

SANITIZE AWAY 
isopropyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50241-406
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.72 L  in 1 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50241-406-00	3.785 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/06/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/06/2020

Labeler - Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. (028311595)

Registrant - Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. (028311595)

Establishment
Name	Address	ID/FEI	Business Operations
Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.		028311595	manufacture(50241-406) , api manufacture(50241-406) , pack(50241-406)