PREFERENCE HAND SANITIZER- alcohol spray

Preference Hand Sanitizer by

Drug Labeling and Warnings

Preference Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Whip Mix Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethanol 72%

Purpose

Liquid Hand Sanitizer

Use

Used by Health Care Professionals for preventing the spread of both pathogenic microorganisms as well as resident bacterial flora and reducing healthcare-associated infections.

Warnings

Flammable, Keep away from fire or flame.

DO NOT USE

For External Use Only

Do not get in the eyes. If splashed in eyes, rinse promptly and thoroughy with water. Discontinue use if irritation and redness develop. If irritation persists for more that 5 days, consult a physician.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

In case of alcohol ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

Apply product liberally on hands and rub together until dry.

Inactive Ingredients

Cyclomethicone, Sodium Lactate, Isopropyl Myristace, Cyclomethicone (and) Trimethyisiloxyl Silicane.

Principal Display Panel

Preference

Liquid Hand Sanitizer

Favored 3:1

over the leanding liquid sanitizer

• Kills 99.9% of most common germs
• Dries in less than 10 seconds
• Moisturizes the skin
• Not harmful to beneficial micro-organisms

INGREDIENTS AND APPEARANCE

PREFERENCE HAND SANITIZER 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62223-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	340.56 mL  in 470 mL

Inactive Ingredients
Ingredient Name	Strength
CYCLOMETHICONE (UNII: NMQ347994Z)
SODIUM LACTATE (UNII: TU7HW0W0QT)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62223-001-16	470 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/23/2020
2	NDC: 62223-001-32	950 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/23/2020

Labeler - Whip Mix Corporation (006385173)

Establishment
Name	Address	ID/FEI	Business Operations
Whip Mix Corporation		006385173	repack(62223-001) , manufacture(62223-001) , relabel(62223-001)