TRIDERGEL- benzalkonium chloride gel 
Trifluent Pharma LLC

----------

TRIDERGEL™

Drug Facts

Active Ingredients

Benzalkonium Chloride (0.1%)

Purpose

Antimicrobial

Indications for management of:

Warnings

For external use only.

When using this product avoid contact with eyes; rinse immediately with cool tap water if contact occurs.

Do not use more than the recommended dose or longer than prescribed without checking with your physician. Talk with your physician before you use any other medicines or cleansers on your skin. Ask your physician before prolonged sun exposure. If your symptoms do not improve or they worsen, contact your physician

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Directions

Inactive Ingredients

Aloe Barbadensis Leaf Juice Extract, Aminomethyl Propanol, Butylparaben, Carbomer, Decyl Glucoside, Ethylparaben, Glycerin, Hydrolyzed Eggshell Membrane, Isobutylparaben, Methylparaben, Phenoxyethanol, Propylparaben, Purified Water, Sodium Hyaluronate.

QUESTIONS OR COMMENTS

CALL (210) 944-6920

PRINCIPAL DISPLAY PANEL - 29.6 mL Bottle Label

TRIFLUENT
PHARMA®

TRIDERGEL™
WOUND CARE GEL

BENZALKONIUM CHLORIDE

IN A GEL CONTAINING
TRANSFORMING GROWTH
FACTOR – β

NDC 73352-520-01

1.0 FL OZ (29.6 mL)

PRODUCT SHOULD BE ADMINISTERED
UNDER THE SUPERVISION OF A
LICENSED MEDICAL PRACTITIONER

PRINCIPAL DISPLAY PANEL - 29.6 mL Bottle Label
TRIDERGEL 
benzalkonium chloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73352-520
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
EGG SHELL MEMBRANE (UNII: N7QBR4212V)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
GLYCERIN (UNII: PDC6A3C0OX)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
ETHYLPARABEN (UNII: 14255EXE39)  
ISOBUTYLPARABEN (UNII: 0QQJ25X58G)  
BUTYLPARABEN (UNII: 3QPI1U3FV8)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73352-520-0129.6 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product12/11/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH DRUGM00512/11/2023
Labeler - Trifluent Pharma LLC (117167281)

Revised: 12/2023
Document Id: b947f7ae-c91f-49d3-9090-e316efb535f7
Set id: f12d9e8c-1d69-49d9-a9e9-a392c681aa6c
Version: 1
Effective Time: 20231208
 
Trifluent Pharma LLC