PURESAN ANTIBACTERIAL FOAMING HAND WASH- chloroxylenol liquid 
Avro Enterprises LLC

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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Puresan Foaming Hand Wash

Drug Facts

Active ingredient

Chloroxylenol 0.3% w/w

Purpose

Antiseptic

Uses

  • Handwash to help reduce bacteria on the skin that potentially can cause disease.
  • Recommended for repeated use.

Warnings

For external use only.

When using this product Keep out of eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develop or if 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 with water and dispense sufficient amount of product into cupped palm of hand.
  • Wash both hands thoroughly for 15 seconds.
  • Rinse under running water and dry thoroughly.

Inactive ingredients Water, Sodium Laureth Sulfate, Cocamide DEA, DMDM Hydantoin, Ethyl Alcohol, Phenoxyethanol, Isopropyl Alcohol, Fragrance, FD&C Red 4

Distributed By: Puresan

24 Ames Blvd., Hamburg, NJ 07419

855.500.8080 • puresanusa.com

Antibacterial

Foaming Hand Wash

0.3% Chloroxylenol

33.8 fl. oz. (1000 mL) Refill Bag FOAM

73062-511 Foam Handwash

PURESAN ANTIBACTERIAL FOAMING HAND WASH 
chloroxylenol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73062-511
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
COCO DIETHANOLAMIDE (UNII: 92005F972D)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
ALCOHOL (UNII: 3K9958V90M)  
FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73062-511-011000 mL in 1 BAG; Type 0: Not a Combination Product08/20/202107/20/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/20/202107/20/2024
Labeler - Avro Enterprises LLC (804030166)

Revised: 1/2023
Document Id: f27988e1-47f7-be4c-e053-2a95a90ab398
Set id: ca045eaa-e32d-bbc6-e053-2995a90aaa31
Version: 2
Effective Time: 20230102
 
Avro Enterprises LLC