FDA.reportPublic FDA data

Kay RTU Foaming AB HandSoap

Manufacturer
Kay Chemical Co.
Effective date
2025-03-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:40:48

Label at a glance#

ProductKay RTU Foaming AB HandSoap
Active ingredientCHLOROXYLENOL
Label structure9 sections

Indications and uses

for handwashing to decrease bacteria on the skin.

Dosage and administration

Wet hands to remove soil Dispense palmful spread to cover hands, rub in well air dry, do not rinse or towel dry

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.5%

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

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

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

  • Skin irritation or redness occurs for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands to remove soil
  • Dispense palmful
  • spread to cover hands, rub in well
  • air dry, do not rinse or towel dry

Other Information

REFERENCES SECTION

  • for additional information, see Safety Data Sheet (SDS)
  • EMERGENCY HEALTH INFORMATION: 1 877 231 2615. If located outside the United States and Canada, call collect 952 853 1713 (number is in the US).

INACTIVE INGREDIENT SECTION

Inactive ingredients water (aqua), potassium cocoate, hexylene glycol, sodium sulfate, tetrasodium EDTA, sodium lauryl sulfate, glycerin, caprylyl/capryl glucoside, fragrance, lauryl glucoside, red 40, methylchloroisothiazolinone, yellow 5, methylisothiazolinone

OTC - QUESTIONS SECTION

Questions?  Call 1-800-529-5458

Principal display panel and representative label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ECOLAB

Kay RTU Foaming AB Hand Soap

Active Ingredient: Chloroxylenol 0.5%

1200 mL

(40.6 US FL OZ)

1112847

Kay Chemical Company · 8300 Capital Drive

Greensboro, NC 27409-9790 USA

Customer Service: (800) 529-5458

©2025 Kay Chemical Company

All rights reserved

KUSA · 783800/8000/0225

representative labelrepresentative label

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63146-321KAY RTU FOAMING AB HANDSOAP (CHLOROXYLENOL) SOLUTION [KAY CHEMICAL CO.]1Unmatched20250306_5113f06c-df88-4409-9d09-06dc9ff7b5fa.zip

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
63146-32163146-321-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
CHLOROXYLENOL0F32U78V2QACTIB
WATER059QF0KO0RIACT
POTASSIUM COCOATEF8U72V8ZXPIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
SODIUM SULFATE0YPR65R21JIACT
EDETATE SODIUMMP1J8420LUIACT
SODIUM LAURYL SULFATE368GB5141JIACT
GLYCERINPDC6A3C0OXIACT
CAPRYLYL/CAPRYL GLUCOSIDEE00JL9G9K0IACT
LAURYL GLUCOSIDE76LN7P7UCUIACT
FD&C RED NO. 40WZB9127XOAIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT

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
1b67d0b8-34af-4389-a565-d13ebfe6e1b85113f06c-df88-4409-9d09-06dc9ff7b5fa2025-12-31WarningsExact identifier
spl set id: 5113f06c-df88-4409-9d09-06dc9ff7b5fa

Reported adverse events (FAERS/openFDA)#

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