TRICLARA- benzalkonium chloride liquid

TriClara by

Drug Labeling and Warnings

TriClara by is a Otc medication manufactured, distributed, or labeled by Nightingale Pharmaceuticals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

ACTIVE INGREDIENT

Active Ingredient

Benzalkonium Chloride (0.13%)

PURPOSE

Purpose

Antiseptic - First Aid

INDICATIONS & USAGE

Uses

• treatment of cold sore / fever blister
• effective relief of symptoms of cold sore / fever blister
• protects against infections in sores, burns, cuts and scrapes

WARNINGS

Warnings

• For external use only: Do not use in or around eyes or ears. Consult a physician before using on puncture wounds, serious burns or animal bites.
• Allergy alert: Do not use if you are allergic to any ingredients in this product.

STOP USE

Stop use and consult a doctor if the condition persists or gets worse.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact poison control at 1-800-222-1222.

DOSAGE & ADMINISTRATION

Directions

• clean the affected area with soap and water and thoroughly dry the area.
• for best results apply a small quantity with a rubbing motion 8 times (once every 2 hours while awake) daily at onset of symptoms until cleared.
• wash hands after applying.
• do not share this product with others.
• retain these directions for help with use.
• for use on children under 12 years: ask a doctor.

OTHER SAFETY INFORMATION

Other information

• Store at 15 to 25°C (59 to 77°F), in a dry place, away from heat, humidity and direct sunlight
• Discard 30 days after removeal from vauumed pouch.

INACTIVE INGREDIENT

Inactive ingredients

glycerin, water, N-acetyl cysteine, sodium hydroxide (for pH), ascorbic acid

PRINCIPAL DISPLAY PANEL

TriClara ® ON & GONE

New

Antiseptic Cold Sore Treatment

0.13% Benzalkonium Chloride

FAST

CLEAR

EFFECTIVE

BETTER APPEARANCE + SOOTHING RELIEF

Cold Sore / Fever Blister Antiseptic

NET WT 3.5G / .12 OZ

Distributed by:

Nightingale Pharmaceuticals, Inc.

Santee, CA 92071

www.triclara.com

RETAIN CARTON FOR COMPLETE PRODUCT INFORMAITON

INGREDIENTS AND APPEARANCE

TRICLARA 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72518-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
ACETYLCYSTEINE (UNII: WYQ7N0BPYC)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
ASCORBIC ACID (UNII: PQ6CK8PD0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72518-001-00	3.5 g in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/14/2019

Labeler - Nightingale Pharmaceuticals, Inc. (081338827)