PROPOWER ORIGINALS ANTIMICROBIAL FOAMING SO AP- chloroxylenol liquid 
BUNZL

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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ProPower Originals Antimicrobial Foaming Soap

Active ingredient

Chloroxylenol 0.5%

Purpose

Antimicrobial

Use

Warnings

For external use only

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Inactive ingredients

Water (Aqua), Alcohol, Lauric Acid, Ethanolamine, Dipropylene Glycol, Lactic Acid, Poloxamer 124, Isopropyl Alcohol, Sodium Metabisulfite, Sodium Sulfite, Tetrasodium EDTA, Sodium Sulfate, Fragrance (Parfum), Methylparaben, Propylparaben, Green 3 (CI 42053), Red 33 (CI 17200)

Product Label

PROPOWER ORIGINALS ANTIMICROBIAL FOAMING SO AP 
chloroxylenol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66294-521
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.005 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
LAURIC ACID (UNII: 1160N9NU9U)  
MONOETHANOLAMINE (UNII: 5KV86114PT)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
LACTIC ACID (UNII: 33X04XA5AT)  
POLOXAMER 124 (UNII: 1S66E28KXA)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
SODIUM SULFITE (UNII: VTK01UQK3G)  
EDETATE SODIUM (UNII: MP1J8420LU)  
SODIUM SULFATE (UNII: 0YPR65R21J)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66294-521-401200 mL in 1 BOTTLE; Type 0: Not a Combination Product05/15/2015
2NDC:66294-521-421250 mL in 1 BOTTLE; Type 0: Not a Combination Product05/15/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/15/2015
Labeler - BUNZL (799540588)

Revised: 11/2022
Document Id: f867e114-c71e-45b5-b007-b0b6889f6c46
Set id: 0d9210a6-41dc-47e6-af00-0a2f4db35754
Version: 3
Effective Time: 20221116
 
BUNZL