CHEMSTAR Foaming Hand Sanitizer by Kay Chemical Company Drug Facts

Drug Details [pdf]

CHEMSTAR FOAMING HAND SANITIZER- benzalkonium chloride solution
Kay Chemical Company

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Drug Facts

Active ingredient

Benzalkonium chloride 0.1%

Purpose

Antiseptic handwash

for handwashing to decrease bacteria on skin

Warnings

For external use only

Do not use

in eyes

When using this product

if in eyes, rinse promptly and throughly with water
discontinue use if irritation and redness develop

Stop use and ask doctor if

skin irritation or redness persists 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

wash 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)
For emergency medical information in USA, call (877) 231-2615 or call collect 0 (952) 853-1713

Inactive ingredients water (aqua), isopropyl alcohol, propylene glycol, CI 16035 (FD&C Red 40), CI 42090 (FD&C Blue 1)

Questions? call 1-800-529-5458

Principal Display Panel and Representative label

CHEMSTAR

Foaming

Hand Sanitizer

Sanitizante de manos en espuma

KEEP OUT OF REACH OF CHILDREN

FOR INSTITUTIONAL USE ONLY

Benzalkonium chloride 0.1%

Net Contents: 42 US fl oz (1250 ml)

1111302

Distributed by:

Kay Chemical Company

8300 Capital Drive Greensboro, NC 27409

Made in USA CSUSA 778273/8000/0621

representative label

CHEMSTAR FOAMING HAND SANITIZER
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63146-316
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: 63146-316-10	1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/08/2021	12/31/2025

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	12/08/2010	12/31/2025

Labeler - Kay Chemical Company (003237021)

Revised: 12/2025

Document Id: 4020780e-588f-409b-9ff3-cb244864e6c4

Set id: a49da436-fb0b-41bf-80b8-d52e11cb09f2

Version: 4

Effective Time: 20251231