FORTICEPT MAXI WASH- benzalkonium chloride liquid

Forticept Maxi Wash by

Drug Labeling and Warnings

Forticept Maxi Wash by is a Animal medication manufactured, distributed, or labeled by Lidan, Inc., Cosco International, Inc., Pharmex Group, LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzakonium Chloride............0.13%

Inactive ingredients:

Detergents, botanical extracts, and preservatives……………………………………………..……….99.87%

Uses

Helps remove dirt and debris. Can be used in the treatment of wounds, superficial minor skin irritations. Effective against both gram-negative and gram-positive bacteria, ringworm, protozoa and some viruses. Rapid acting with a moderately long duration of action. Topical antiseptic to help decrease the risk of infection.

Warnings

For external use only * Not for human use * Keep out of reach of children

When using this product- avoid eye contact.

Stop use and ask a veterinarian if condition worsens, symptoms last more than 7 days or clear up and occur again within a few days.

Directions for use:

Spray on affected area or wound. Do not wash or wipe off. Apply 1-2 times per day or as needed until the area is healed. Will not burn, sting or irritate. For skin and wound areas that need to be cleaned apply treatment until you reach desired condition.

Storage and handling:

Keep container closed when not in use. Do not store below 32°F/0°C or above 95°F/35°C for extended periods of time. In case of spill, flood with water.

FIRST AID

Eye contact:  In case of contact, immediately flush eyes with cool running water. 

Skin contact: Wash the skin with water and soap. Wash clothing before reuse.

Ingestion: If large quantities of this material are swallowed, contact poison control center immediately!

118 mL Label

240 mL Label

473 mL Label

946 ml Label

INGREDIENTS AND APPEARANCE

FORTICEPT MAXI WASH 
benzalkonium chloride liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 72127-0704
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
benzalkonium chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	benzalkonium chloride	1.3 g  in 1000 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72127-0704-0	118 g in 1 BOTTLE, SPRAY
2	NDC: 72127-0704-1	240 g in 1 BOTTLE, SPRAY
3	NDC: 72127-0704-2	473 g in 1 BOTTLE, SPRAY
4	NDC: 72127-0704-3	946 g in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/29/2016

Labeler - Lidan, Inc. (014456716)

Registrant - Lidan, Inc. (014456716)

Establishment
Name	Address	ID/FEI	Business Operations
Cosco International, Inc.		016433141	api manufacture, manufacture, analysis, pack

Establishment
Name	Address	ID/FEI	Business Operations
Pharmex Group, LLC.		365309015	pack, repack