EXP Foaming Hand Sanitizer by Kay Chemical Company Drug Facts

Drug Details [pdf]

EXP FOAMING HAND SANITIZER - benzalkonium chloride solution
Kay Chemical Company

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Drug Facts

Active ingredient

Benzalkonium chloride 0.1%

Purpose

Antiseptic handwash

Uses

for handwashing to decrease bacteria on the skin

Warnings

For external use only

Do not use

in eyes

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.

Direction

wet hands thoroughly with product and allow to dry without wiping.
do not use if hands are visibly dirty or greasy; wash hands with soap and water instead.

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), isopropyl alcohol, propylene glycol, FD&C red 40, FD&C blue 1

Questions? call 1-800-529-5458

Principal display panel and representative label

ECOLAB

NDC: 63146-320-16

EXP Foaming

Hand Sanitizer

Active Ingredient: Benzalkonium chloride 0.1%

1200 mL

(40.6 US FL OZ) 1112848

Kay Chemical Company · 8300 Capital Drive

Greensboro, NC 27409-9790 USA

Customer Service: (800) 529-5458

KUSA

782982/8000/0224

representative label

EXP FOAMING HAND SANITIZER
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63146-320
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 mg in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC: 63146-320-16	1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2024	12/31/2025

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	07/01/2024	12/31/2025

Labeler - Kay Chemical Company (003237021)

Revised: 12/2025

Document Id: b5109822-6a0d-4bdb-9a23-81bad420f110

Set id: c9c6deae-380d-4796-8513-77c0c2e6dd8d

Version: 2

Effective Time: 20251231