FORTICEPT ANTI-ITCH EAR DROPS- hydrocortisone 1% medicated otic solution liquid

Forticept Anti-Itch Ear Drops by

Drug Labeling and Warnings

Forticept Anti-Itch Ear Drops by is a Animal medication manufactured, distributed, or labeled by Lidan, Inc., Cosco International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s):

Hydrocortisone........1% (Anti-Itch)

Indications:

Helps relive itching associated with minor skin irritations, inflammation, and rashes.

Warnings:

For external use only / Not for human use
Keep out of reach of children - if swallowed, get medical help or contact a Poison Control Center right away.
When using this product - Avoid contact with eyes
Stop use and ask a veterinarian if condition worsens, symptoms persist for more than 7 days, or clear up and occur again with a few days, and do not begin use of any other hydrocortisone product unless you have asked a doctor.

Directions:

Pre-clean ear with Forticept® Antiseptic Ear Flush. Apply solution to the ear canal and with firm but gentle pressure, massage the base of the ear.

Storage:

Store at room temperature. Protect from freezing or excessive heat.

Inactive Ingredients:

Propylene Glycol, Glycerin, Water, Carbamide, Polysorbate 20, Povidone-iodine, Benzyl Alcohol, Boric Acid

Questions:

+1(470) 736-8166

Lidan, Inc., Kennesaw, GA  30152 USA

www.forticept.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FORTICEPT ANTI-ITCH EAR DROPS 
hydrocortisone 1% medicated otic solution liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 72127-0906
Route of Administration	AURICULAR (OTIC)

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE	10 g  in 1000 g

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
UREA (UNII: 8W8T17847W)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
POVIDONE-IODINE (UNII: 85H0HZU99M)
BENZYL ALCOHOL (UNII: LKG8494WBH)
BORIC ACID (UNII: R57ZHV85D4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72127-0906-1	60 g in 1 BOTTLE, DISPENSING

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/20/2022

Labeler - Lidan, Inc. (014456716)

Registrant - Lidan, Inc. (014456716)

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