PRO FORMANCE PLUM PERFECTION ANTIBACTERIAL FOAM S OAP- benzalkonium chloride liquid 
Pro-Link, 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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Pro Formance™ Plum Perfection Antibacterial Foam Soap

Active ingredient

Benzalkonium Chloride 0.5%

Purpose

Antimicrobial

Uses

• Handwash to help decrease bacteria on the skin

• Recommended for repeated 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

• Wet hands

• Apply a small amount of product and work into a lather

• Rinse well and dry hands completely

Inactive Ingredients

Water (Aqua), Propylene Glycol, Glycerin, Cocamidopropyl Betaine, PEG-80 Sorbitan Laurate, Citric Acid, Ethylhexylglycerin, Lauramine Oxide, Polyquaternium-10, Fragrance (Parfum), Phenoxyethanol, Blue 1 (CI 42090), Red 33 (CI 17200)

Product LabelProduct Label

PRO FORMANCE PLUM PERFECTION ANTIBACTERIAL FOAM S OAP 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66908-401
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) Benzalkonium Chloride0.005 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Propylene Glycol (UNII: 6DC9Q167V3)  
Glycerin (UNII: PDC6A3C0OX)  
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)  
PEG-80 Sorbitan Laurate (UNII: 239B50Y732)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Ethylhexylglycerin (UNII: 147D247K3P)  
Lauramine Oxide (UNII: 4F6FC4MI8W)  
POLYQUATERNIUM-10 (10000 MPA.S AT 2%) (UNII: PI1STR9QYH)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66908-401-401200 mL in 1 PACKAGE; Type 0: Not a Combination Product02/28/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E02/28/2018
Labeler - Pro-Link, Inc. (144650637)

Revised: 11/2022
Document Id: 8d9fc145-b3ae-4c5f-8b9d-39bc349edec3
Set id: 6bdc6f78-5ecd-4de7-9457-eda580c3a3e0
Version: 2
Effective Time: 20221115
 
Pro-Link, Inc.