POWER FORCE ANTIBACTERIAL HANDSOAP CITRUS SCENT- chloroxylenol liquid

POWER FORCE ANTIBACTERIAL HANDSOAP CITRUS SCENT by

Drug Labeling and Warnings

POWER FORCE ANTIBACTERIAL HANDSOAP CITRUS SCENT by is a Otc medication manufactured, distributed, or labeled by KOREX CHICAGO LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Chloroxylenol 0.3%

Purpose

Antibacterial

Use

for handwashing to decrease bacteria on the skin.

Warnings

For external use only.

Do not use in eyes.

When using this product keep out of eyes. If in eyes, rinse promptly and thoroughly with water.

Stop use and ask a 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

 Wet hands and forearms.
 Apply 5 mL or palmful to hands and forearms.
 Scrub thoroughly for 30 seconds and rinse.

Inactive ingredients

Water, sodium laureth sulfate, sodium lauryl sulfate, lauramine oxide, propylene glycol, sodium chloride, fragrance, sodium xylene sulfonate, citric acid, D&C Orange No. 4, methylisothiazolinone, methylchloroisothiazolinone. Contains fragrance allergen.

Questions?

Call 844-484-0332

SPL UNCLASSIFIED SECTION

TOUGH ON GREASE

​ULTRA DISHWASHING LIQUID

Compare to Dawn Ultra*

Do not add bleach. Not for use in dishwashers. 
Product Not Tested On Animals.
www.aldi.us

Ultra Concentrated

*This product is not manufactured or distributed by Procter & Gamble, distributor of Dawn Ultra Antibacterial Hand Soap

DIST. & SOLD
EXCLUSIVELY BY: ALDI
BATAVIA, IL 60510

Packaging

INGREDIENTS AND APPEARANCE

POWER FORCE ANTIBACTERIAL HANDSOAP CITRUS SCENT 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73487-009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	0.3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
D&C ORANGE NO. 4 (UNII: Q1LIY3BO0U)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)

Product Characteristics
Color		Score
Shape		Size
Flavor	CITRUS	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73487-009-01	709 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/15/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	09/15/2025

Labeler - KOREX CHICAGO LLC (792133147)

Establishment
Name	Address	ID/FEI	Business Operations
KOREX CHICAGO LLC		792133147	manufacture(73487-009) , analysis(73487-009)