Thursday, 23 August 2012

Naphcon



naphazoline hydrochloride

Dosage Form: Ophthalmic Solution

DESCRIPTION


Naphcon® FORTE (Naphazoline Hydrochloride Ophthalmic Solution USP), 0.1% is a sterile preparation. Naphazoline HCl, an ocular vasoconstrictor, is an imidazoline derivative sympathomimetic amine. It occurs as a white, odorless crystalline powder having a bitter taste and is freely soluble in water and in alcohol. The active ingredient is represented by the structural formula:



C14H14N2HCl


MW=246.74


Chemical name:


2-(1-naphthylmethyl)-2-imidazoline monohydrochloride


Each mL contains: Active: Naphazoline Hydrochloride 0.1%. Preservative: Benzalkonium Chloride 0.01%. Inactives: Boric Acid, Sodium Chloride, Potassium Chloride, Edetate Disodium, Sodium Carbonate and/or Hydrochloric Acid (to adjust pH), Purified Water. DM-00


The solution has a pH of 5.5 to 7.0.



CLINICAL PHARMACOLOGY


Naphazoline constricts the vascular system of the conjunctiva. It is presumed that this effect is due to direct stimulation action of the drug upon the alpha adrenergic receptors in the arterioles of the conjunctiva resulting in decreased conjunctival congestion. Naphazoline belongs to the imidazoline class of sympathomimetics.



INDICATIONS AND USAGE


Naphcon® FORTE (Naphazoline Hydrochloride Ophthalmic Solution USP), 0.1% is indicated for use as a topical ocular vasoconstrictor.



CONTRAINDICATIONS


Contraindicated in the presence of an anatomically narrow angle or in narrow angle glaucoma or in persons who have shown hypersensitivity to any component of this preparation.



WARNINGS


NOT FOR INJECTION – FOR OPHTHALMIC USE ONLY. Patients under therapy with MAO inhibitors may experience a severe hypertensive crisis if given a sympathomimetic drug. Use in children, especially infants, may result in CNS depression leading to coma and marked reduction in body temperature.


Remove contact lenses before using.



PRECAUTIONS



General


For topical ophthalmic use only. Use with caution in the presence of hypertension, cardiovascular abnormalities, hyperglycemia (diabetes), hyperthyroidism, infection or injury.



Information for Patients


Patients should be advised to discontinue the drug and consult a physician if relief is not obtained within 48 hours of therapy, if irritation, blurring or redness persists or increases, or if symptoms of systemic absorption occur, i.e., dizziness, headache, nausea, decrease in body temperature, or drowsiness.


To prevent contaminating the dropper tip and solution, do not touch the eyelids or the surrounding area with the dropper tip of the bottle. If solution changes color or becomes cloudy, do not use.



Drug Interactions


Concurrent use of maprotiline or tricyclic antidepressants and naphazoline may potentiate the pressor effect of naphazoline. Patients under therapy with MAO inhibitors may experience a severe hypertensive crisis if given a sympathomimetic drug. (See WARNINGS.)



Pregnancy Category C


Animal reproduction studies have not been conducted with naphazoline. It is also not known whether naphazoline can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Naphazoline should be given to a pregnant woman only if clearly needed.



Nursing Mothers


It is not known whether naphazoline is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when naphazoline is administered to a nursing woman.



Pediatric Use


Safety and effectiveness in pediatric patients have not been established. See “WARNINGS” and “CONTRAINDICATIONS.”



ADVERSE REACTIONS


Ocular: Mydriasis, increased redness, irritation, discomfort, blurring, punctuate keratitis, lacrimation, increased intraocular pressure.


Systemic: Dizziness, headache, nausea, sweating, nervousness, drowsiness, weakness, hypertension, cardiac irregularities, and hyperglycemia.



DOSAGE AND ADMINISTRATION


Instill one or two drops in the conjunctival sac(s) every three to four hours as needed.



HOW SUPPLIED


Naphcon® FORTE (Naphazoline Hydrochloride Ophthalmic Solution USP), 0.1% is available in 15 mL in DROP-TAINER® dispenser.


NDC 0998-0079-15.


Storage: Store at 8° - 27°C (46° - 80°F).


Caution: Federal ( USA) law prohibits dispensing without prescription.


ALCON ( Puerto Rico) INC.

Humacao, Puerto Rico 00791 USA


Printed in USA


September 1996


236185








Naphcon 
naphazoline hydrochloride  solution










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)0998-0079
Route of AdministrationOPHTHALMICDEA Schedule    





























INGREDIENTS
Name (Active Moiety)TypeStrength
naphazoline hydrochloride (naphazoline)Active1 MILLIGRAM  In 1 MILLILITER
benzalkonium chlorideInactive 
boric acidInactive 
sodium chlorideInactive 
potassium chlorideInactive 
edetate disodiumInactive 
sodium carbonate and/or hydrochloric acidInactive 
waterInactive 


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      










Packaging
#NDCPackage DescriptionMultilevel Packaging
10998-0079-1515 mL (MILLILITER) In 1 BOTTLE, PLASTICNone

Revised: 09/2006Alcon

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