Kroger® ANTIBACTERIAL Orange ScentHAND SOAP

Kroger ANTIBACTERIAL Orange Scent HAND by

Drug Labeling and Warnings

Kroger ANTIBACTERIAL Orange Scent HAND by is a Otc medication manufactured, distributed, or labeled by Korex Chicago LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

KROGER ANTIBACTERIAL ORANGE SCENT HAND- chloroxylenol soap 
Korex Chicago LLC

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Kroger® ANTIBACTERIAL Orange ScentHAND SOAP

Drug Facts

Active ingredient

Chloroxylenol 0.3%

Purpose

Antibacterial

Use

for handwashing to decrease bacteria on the skin

Warnings

For external use only: hands only

When using this product do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation and redness develop condition 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 palmful to hands and forearms. scrub thoroughly for 30 seconds and rinse.

Inactive ingredients

water, sodium laureth sulfate, sodium lauryl sulfate, lauramine oxide, sodium xylenesulfonate, propylene glycol, citric acid, orange 4, fragrance, methylchloroisothiazolinone, methylisothiazolinone. Contains fragrance allergen.

Kroger®

COMPARE TO DAWN®ULTRA ANTIBACTERIAL

2X CLEANING POWERVERSUS NON-CONCENTRATED DISH SOAPS

GREASE CLEANING

ULTRACONCENTRATED DISH SOAP

Our Brands. Our Guarantee.
Love It or Your Money Back.

www.kroger.com

For More Ingredient Information, Visit www.kroger.com or call 800-632-6900

Do not add bleach. Not for use in dishwashers.

Contains surfactants

Phosphate Free

DISTRIBUTED BY THE KROGER CO.

CINCINNATI, OHIO 45202

*Dawn ®is a registered trademark of The Procter and Gamble Company, Cincinnati, OH 45202. The Procter and Gamble Company is not affiliated with The Kroger Co. or this product.

Packaging

KROGER ANTIBACTERIAL ORANGE SCENT HAND 
chloroxylenol soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73487-006
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)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
D&C ORANGE NO. 4 (UNII: Q1LIY3BO0U)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73487-006-01	828 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2022	02/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/01/2022	02/01/2025

Labeler - Korex Chicago LLC (792133147)

Establishment
Name	Address	ID/FEI	Business Operations
Korex Chicago LLC		792133147	manufacture(73487-006)

Revised: 12/2024

Document Id: 28f1e9f3-d527-82df-e063-6294a90a9de5

34390-5

Set id: 68a5bed3-7ad9-471b-9a29-5492bb4b01a0

Version: 3

Effective Time: 20241210