QSR HAND SANITIZER- alcohol solution

QSR Hand Sanitizer by

Drug Labeling and Warnings

QSR Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Ecolab Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethanol 60% by volume

Purpose

Antiseptic handwash

Uses

• For handwashing to decrease bacteria on 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
• on deep cuts or puncture wounds

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 a 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 HANDWASHING WITH SOAP AND WATER
• For additional information, see Safety Data Sheet (SDS)
• For emergency medical information in USA, call (877) 231-2615 or call collect 0 (952) 853-1713

Inactive ingredients

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

QUESTIONS

Questions? Call 1-800-529-5458

Principal display panel and representative label

KAY

QSR

Hand Sanitizer

FOR INSTITUTIONAL USE ONLY

Ethanol 60% by volume

Net contents: 40.6 US fl oz (1200 mL)

Meets the requirements for Hand Antiseptics as specified in section 2-301.16 of the 2017 Food Code.

(2017 Food Code).

SDS-NC-872, SDS-NJ-20007

Distributed by

Kay Chemical Company

8300 Capital Drive · Greensboro, NC 27409-9790 USA Customer Service: (800) 529-5458

©2020 Kay Chemical Company

All rights reserved | KUSA 756614/8004/1020

INGREDIENTS AND APPEARANCE

QSR HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-673
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
WATER (UNII: 059QF0KO0R)
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: 47593-673-25	800 mL in 1 BAG; Type 0: Not a Combination Product	12/31/2025
2	NDC: 47593-673-56	1200 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/31/2025
3	NDC: 47593-673-95	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/31/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/31/2025

Labeler - Ecolab Inc. (006154611)