CHLOROXYLENOL- chloroxylenol liquid 
Consumer Product Partners, LLC

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Mountain Falls 710.002/710AC rev 1 Citrus Orange Antibacterial Hand Soap

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 Conrol Center right away.

Directions

  • wet hands
  • apply palmful to hands,
  • scrub thoroughly
  • rinse thoroughly

Inactive ingredients

water, sodium C14-16 olefin sulfonate, lauramine oxide, sodium laureth sulfate, sodium lauryl sulfate, isopropylideneglycerol, sodium chloride, alcohol denat., phenoxyethanol, citric acid, methylisothiazolinone, trisodium ethylenediamine disuccinate, fragrance, yellow 5, red 33

Do not add bleach.  Not for use in dishwashers.

​Contains Surfactants. Phosphate Free

disclaimer

This product is not manufactured or distributed by Procter & Gamble, distributor of Dawn Ultra Antibacteial Hand Soap Orange Scent

principal display panel

mountain

falls

*Compare

to Dawn

tough

on

grease

ultra

concentrated

cleaning

power

dish soap

antibacterial hand soap

orange scent

24 FL OZ (710 mL)

mm3

CHLOROXYLENOL 
chloroxylenol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11344-710
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL3.09 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
SOLKETAL (UNII: 3XK098O8ZW)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
ALCOHOL (UNII: 3K9958V90M)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11344-710-50710 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/14/201710/05/2019
2NDC:11344-710-571183 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/14/201710/05/2019
3NDC:11344-710-511770 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/14/201710/05/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)01/14/201710/05/2019
Labeler - Consumer Product Partners, LLC (119091520)
Registrant - Consumer Product Partners, LLC (119091520)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(11344-710)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(11344-710)

Revised: 2/2024
Document Id: 10bdeb4d-4d1b-bf03-e063-6394a90ac0a5
Set id: 83199ad4-1a9a-47d8-896d-4f0922312a34
Version: 25
Effective Time: 20240206
 
Consumer Product Partners, LLC