HAND SANITIZER- alcohol liquid

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Essity Professional Hygiene North America LLC, Vi-Jon, LLC, Vi-Jon, LLc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl alcohol 70% v/v

Purpose

Antiseptic

Uses

Handwash to help reduce bacteria on the skin

Warnings

For external use only: hands

Flammable.  Keep away from fire or flame.

When using this product

• keep out of eyes. In case of contact with eyes, flush thoroughly with water.
• avoid contact with broken skin
• do not inhale or ingest

Stop use and ask a doctor if

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

Keep out of reach children

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

Directions

• wet hands thoroughly with product and allow to dry without wiping
• for children under 6, use only under adult suervision
• not recommended for infants

Other information

• do not store above 105° F
• may discolor some fabrics
• harmful to wood finishes and plastics

Inactive ingredients

water, PEG-8 Dimethicone, meadowfoamamidopropyl betaine, glyceryl caprylate/caprate, glycerin, tocopheryl acetate, isopropyl Myristate

Questions or Comments?

1-866-722-8675

Principal display panel

NDC: 49351-301-01

TORK HAND SANITIZER

Alcohol Foam

Ethyl alcohol, 70% v/v

UL Ecologo Product certified for reduced environmental impact: View specific attributes evaluated: UL.comel UL 2783

NSF Nonfood compounds program Listed E3 registration #157039

For commercial use.

Essity

Manufactured for Essity Professional Hygiene North America LLC

2929 Arch Street

Philadelphia, PA 19104

www.essity.com, www.torkusa.com

Patents www.essity.com/patents

SDS-MO-15036, SDA WI-2486, DSP-MO-28, DSP-MO-34

Pat. 9,161,982

Peel here for drug facts

1 L (33.8 US FL OZ)

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49351-301
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	.70 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
PEG-8 DIMETHICONE (UNII: GIA7T764OD)
MEADOWFOAMAMIDOPROPYL BETAINE (UNII: HNV0L650LG)
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49351-301-01	1000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	01/06/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/06/2020

Labeler - Essity Professional Hygiene North America LLC (005694349)

Registrant - Vi-Jon, Inc (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon, Inc		150931459	manufacture(49351-301)