First Mark Ultra Hand Sanitizer Liquid
FDA Label NDC 51042-002

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Performance Food Group for the product First Mark Ultra Hand Sanitizer (NDC 51042-002). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, do not use, when using this product, otc - ask doctor, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

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

Otc - Ask Doctor

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

Otc - 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.

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

Representative Label (Label)

Representative Label (Label)

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