FIRST MARK ULTRA HAND SANITIZER- alcohol liquid

FIRST MARK ULTRA HAND SANITIZER by

Drug Labeling and Warnings

FIRST MARK ULTRA HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Performance Food Group. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 60% v/v

Purpose

Antiseptic handwash

Uses

• For handwashing to decrease bacteria on the skin

Warnings

• For external use only
• FLAMMABLE, keep away from fire or flame, heat, sparks and sources of static discharge

Do not use

• In eyes

When using this product

• If in eyes, rinse promptly and thoroughly with water
• Discontinue use if irritation and redness develop

Stop use and ask a doctor if eye or skin irritation or redness occurs for more than 72 hours

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

Directions

• Apply liberal amount into hand
• Spread by rubbing hands together
• Rub to dryness with attention to area around nails and between fingers

Other information

• THIS PRODUCT IS NOT A SUBSTITUTE FOR HANDWASHINGWITH SOAP AND WATER
• For additional information, see Safety Data Sheet (SDS)
• EMERGENCY HEALTH INFORMATION: In the US, call (833) 571-1403

INACTIVE INGREDIENT

Inactive ingredients water (aqua), isopropyl alcohol, triethanolamine, acrylates/C10-30 alkyl acrylate crosspolymer, propylene glycol, myristyl alcohol

Principal display panel and representative label

REORDER # 644086

1111219 778372

778372/7300/0521

FIRST

MARK

The Mark of Quality In 

Non-Food Essentials

ULTRA

HAND

SANITIZER

Active Ingredient: Ethanol 60% by volume

SDS-NC-872, SDS-NJ-20007

40.6 US fl. oz. (1200 mL)

Meets the requirements for

Hand Antiseptics as specified

in section 2-301.16 of the

2017 Model Food Code.

Made in the USA

DISTRIBUTED BY:

PERFORMANCE FOOD GROUP

12500 WEST CREEK PARKWAY

RICHMOND, VIRGINIA 23238

INGREDIENTS AND APPEARANCE

FIRST MARK ULTRA HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51042-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	60 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
Propylene glycol (UNII: 6DC9Q167V3)
MYRISTYL ALCOHOL (UNII: V42034O9PU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51042-002-09	1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/21/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/21/2021

Labeler - Performance Food Group (127038714)