CHEMSTAR by Kay Chemical Co. Drug Facts

CHEMSTAR by

Drug Labeling and Warnings

CHEMSTAR by is a Otc medication manufactured, distributed, or labeled by Kay Chemical Co.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CHEMSTAR- 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 and forearms
• dispense a palmful to hands and forearms
• scrub thoroughly 
• Rinse and 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 ingredientsWater (Aqua), Potassium Cocoate, Hexylene Glycol, Sodium Sulfate, Tetrasodium EDTA, Sodium lauryl sulfate, Glycerin, Sodium Citrate, Glyceryl Oleate, fragrance, sodium glycolate, caprylyl/capryl glucoside, Lauryl Glucoside, Magnesium Nitrate, Sodium Hydroxide, Methylchloroisothiazolinone, Magnesium Chloride, Yellow 5, Methylisothiazolinone, Red 4

Questions? call 1.800.529-5458

Principal display panel and representative label

CHEMSTAR 

Foaming Antibacterial 

Hand Soap

KEEP OUT OF REACH OF CHILDREN

Chloroxylenol 0.5%

Net Contents 42 US fl ox (1250 mL)

111280

Distributed by: Kay Chemical Company

8300 Capital Drive - Greensboro, NC 27409

Made in USA

CSUSA 779394/8000/0621

CHEMSTAR 
chloroxylenol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63146-315
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	0.5 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
GLYCERYL OLEATE (UNII: 4PC054V79P)
SODIUM GLYCOLATE (UNII: B75E535IMI)
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63146-315-10	1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/23/2021	12/31/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/23/2021	12/31/2025

Labeler - Kay Chemical Co. (003237021)

Revised: 12/2025

Document Id: 97bbe995-b1ba-4de1-a9dc-66d577ecf60e

34390-5

Set id: 4a3f3cb0-30ea-4483-a0da-ae5952cdb0f8

Version: 4

Effective Time: 20251231