REFRESH PUREBAC FOAM- chloroxylenol liquid 
SC Johnson Professional USA, Inc.

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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Refresh PureBac™ Foam

Drug Facts

Active ingredient

Chloroxylenol, 0.5%

Purpose

Antibacterial

Uses

  • For handwashing to reduce bacteria on the skin

Warnings

For external use only

When using this product

  • avoid contact with eyes. In case of eye contact, flush with water.

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

Directions

  • Apply foaming cleanser to dry hands
  • Rub hands together to spread lather
  • Wash for 15-20 seconds
  • Rinse & dry hands thoroughly

Inactive ingredients

Aqua (Water), Propylene Glycol, TEA-lauryl Sulfate, PPG-24-Glycereth-24, Sodium Laureth Sulfate, Aloe Barbadensis Leaf Juice, Cocamidopropyl Betaine, Allantoin, Tetrasodium EDTA, Citric Acid, Magnesium Nitrate, Magnesium Chloride, Diazolidinyl Urea, Methylparaben, Propylparaben, Methylchloroisothiazolinone, Methylisothiazolinone

PRINCIPAL DISPLAY PANEL - 1 L Bottle Label

SCJ PROFESSIONAL
A family company™

NDC 11084-160-27

Refresh PureBac™ FOAM

ANTIMICROBIAL FOAM SOAP
Dye & Fragrance-Free Antibacterial Foam Handwash

Stock #:PBF1L/4000000752

1 L (33.8 fl oz)

SC Johnson Professional USA, Inc.
Charlotte, NC 28217
1-800-248-7190. www.scjp.com

deb
SKIN CARE

Pat.www.scjp.com/patents

1000002970/1020

PRINCIPAL DISPLAY PANEL - 1 L Bottle Label
REFRESH PUREBAC FOAM 
chloroxylenol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-160
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL5 g  in 1 L
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
TRIETHANOLAMINE LAURYL SULFATE (UNII: E8458C1KAA)  
PPG-24-GLYCERETH-24 (UNII: V341SPY84U)  
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
ALLANTOIN (UNII: 344S277G0Z)  
EDETATE SODIUM (UNII: MP1J8420LU)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11084-160-271 L in 1 BOTTLE, PLASTIC; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)04/15/201510/01/2023
2NDC:11084-160-121.2 L in 1 BOTTLE, PLASTIC; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)04/15/201510/01/2023
3NDC:11084-160-202 L in 1 BOTTLE, PLASTIC; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)04/15/201510/01/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/15/201510/01/2023
Labeler - SC Johnson Professional USA, Inc. (607378015)
Establishment
NameAddressID/FEIBusiness Operations
SC Johnson Professional CA Inc.203765300manufacture(11084-160)

Revised: 12/2022
Document Id: f464debf-c631-489d-8964-af729ef73ec1
Set id: 1a0efb2b-3814-4275-a896-261a655f8639
Version: 4
Effective Time: 20221223
 
SC Johnson Professional USA, Inc.