Kay Hand Sanitizer Foam

Manufacturer
Ecolab Inc.
Effective date
2025-12-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:26:41

Label at a glance#

ProductKay Hand Sanitizer Foam
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

For handwashing to decrease bacteria on the skin

Dosage and administration

Spread thoroughly onto hands and rub until dry

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 54.7 w/w (equivalent to 62.5% v/v)

Purpose

OTC - PURPOSE SECTION

Antiseptic Handwash

Uses

INDICATIONS & USAGE SECTION

  • For handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

  • For external use only
  • Flammable, keep away from fire or flame, heat, sparks and sources of static discharge.
  • Contents under pressure. Do not store at temperatures above 120°F (48°C), puncture or incinerate
  • Operate only with spout pointing down

Do not use

OTC - DO NOT USE SECTION

  • In eyes

When using this product

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Spread thoroughly onto hands and rub until dry

Other Information

OTHER SAFETY INFORMATION

  • for additional information, see Safety Data Sheet (SDS)
  • Medical Emergency: (877) 231-2615 or call collect 0 (952) 853-1713

INACTIVE INGREDIENT SECTION

Inactive Ingredients water (aqua), isobutane, glycerin, cetearyl alcohol, hydrofluorocarbon 152A, propane, polysorbate-60, sodium lauroyl lactylate, steareth-20, sodium benzoate, tert-butyl alcohol, denatonium benzoate

OTC - QUESTIONS SECTION

Questions? Call 1-800-529-5458

Representative Label and Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KAY®

Hand Sanitizer Foam

Net Contents: 425 g (15 oz)

Active Ingredient: 54.7% w/w (equivalent to 62.5% v/v)

1110978

ECOLAB

This product may be patented | Este producto

puede ser patentado: www.ecolab.com/patents

Distributed by | Distribuido por:

Kay Chemical Company · 8300 Capital Drive

Greensboro, NC 27409-9790 USA

Customer Service: (800) 529-5458

©2022 Kay Chemical Company

All rights reserved | Todas los derechos reservados

Made in USA | Hecho en Estados Unidos

822113 • KUSA 775938/8001/1122

Representative LabelRepresentative Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039465ethanol 62.5 % Topical FoamPSN1
1039465ethanol 0.625 ML/ML Topical FoamSCD1
1039465ethanol 62.5 % Topical FoamSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47593-683-96Kay Hand Sanitizer Foam425 g in 1 CANSOLUTION4251

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47593-68347593-683-96

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Kay Hand Sanitizer FoamETHYL ALCOHOLEcolab Inc.f82eaaaf-cead-497a-8b95-9668310511872025-12-17WarningsExact identifier
ndc (package): 47593-683-96
ndc (product): 47593-683
ndc11 (package): 47593068396
spl id: 4f23f243-888d-4d54-98d0-e500946fe0f8
spl set id: f82eaaaf-cead-497a-8b95-966831051187

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.