Kay RTU Foaming AB HandSoap by Kay Chemical Co. Drug Facts

Drug Details [pdf]

KAY RTU FOAMING AB HANDSOAP- chloroxylenol solution
Kay Chemical Co.

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Drug Facts

Active ingredient

Chloroxylenol 0.5%

Purpose

Antiseptic Handwash

Uses

for handwashing to decrease bacteria on the skin.

Warnings

For external use only

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

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

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

Other Information

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 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

Questions? Call 1-800-529-5458

Principal display panel and representative label

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

KUSA · 783800/8000/0225

representative label

KAY RTU FOAMING AB HANDSOAP
chloroxylenol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63146-321
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	5 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
POTASSIUM COCOATE (UNII: F8U72V8ZXP)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
SODIUM SULFATE (UNII: 0YPR65R21J)
EDETATE SODIUM (UNII: MP1J8420LU)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
GLYCERIN (UNII: PDC6A3C0OX)
CAPRYLYL/CAPRYL GLUCOSIDE (UNII: E00JL9G9K0)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
FD&C RED NO. 40 (UNII: WZB9127XOA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC: 63146-321-16	1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/04/2025	12/31/2025

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	03/04/2025	12/31/2025

Labeler - Kay Chemical Co. (003237021)

Revised: 12/2025

Document Id: 1b67d0b8-34af-4389-a565-d13ebfe6e1b8

Set id: 5113f06c-df88-4409-9d09-06dc9ff7b5fa

Version: 2

Effective Time: 20251231