Naphcon A

Generic Name: naphazoline hydrochloride and pheniramine maleate
Dosage Form: eye drops

Naphcon A®
Eye Drops

For the temporary relief of the minor eye symptoms of itching and redness caused by ragweed, pollen, grass, animal dander and hair.

Naphcon A Description

Active: Naphazoline Hydrochloride 0.025%, Pheniramine Maleate 0.3%. Preservative: Benzalkonium Chloride 0.01%. Inactive: Boric Acid, Edetate Disodium 0.01%, Purified Water, Sodium Borate, Sodium Chloride, Sodium Hydroxide and/or Hydrochloric Acid (to adjust pH). The sterile ophthalmic solution has a pH of about 6 and a tonicity of about 270 mOsm/Kg.

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DIRECTIONS

Put 1 or 2 drops in the affected eye(s) up to 4 times every day.

Warnings

To avoid contamination, do not touch tip of container to any surface. Replace cap after using.

If solution changes color or becomes cloudy, do not use.

Stop use and ask a doctor if you feel eye pain, changes in vision occur, redness or irritation of the eye(s) gets worse or lasts more than 72 hours.

When using this product, pupils may become enlarged temporarily. Overuse may cause more redness of the eye(s). If you are sensitive to any ingredient in this product, do not use. Do not use this product if you have heart disease, high blood pressure, narrow angle glaucoma or trouble urinating unless directed by a physician. Accidental swallowing by infants and children may lead to coma and marked reduction in body temperature. Before using in children under 6 years of age, consult your physician. Keep this and all drugs out of the reach of children. If swallowed, get medical help or contact a Poison  Control  Center right away. Remove contact lenses before using.

Store at 20°- 25°C (68°- 77°F). Protect from light. Use before the expiration date marked on the carton or bottle.

ALCON LABORATORIES, INC.
FORT WORTH, TX  76134  USA
© 2002, 2004, 2005 Alcon, Inc.

Naphcon A 
naphazoline hydrochloride and pheniramine maleate solution/ drops
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:0065-0085
Route of Administration OPHTHALMIC DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
naphazoline hydrochloride (naphazoline) naphazoline 0.25 mg  in 1 mL
pheniramine maleate (pheniramine) pheniramine 3 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
benzalkonium chloride 0.1 mg  in 1 mL
boric acid  
edetate disodium 0.1 mg  in 1 mL
water  
sodium borate  
sodium chloride  
sodium hydroxide and/or hydrochloric acid  
Packaging
# Item Code Package Description
1 NDC:0065-0085-25 2.5 mL (2.5 MILLILITER) in 1 BOTTLE, PLASTIC
2 NDC:0065-0085-15 15 mL (15 MILLILITER) in 1 BOTTLE, PLASTIC
3 NDC:0065-0085-30 30 mL (30 MILLILITER) in 1 BOTTLE, PLASTIC
4 NDC:0065-0085-42 5 mL (5 MILLILITER) in 1 BOTTLE, PLASTIC
5 NDC:0065-0085-38 30 mL (30 MILLILITER) in 1 BOTTLE, PLASTIC
Labeler - ALCON LABORATORIES, INC.
Revised: 08/2006
 
ALCON LABORATORIES, INC.



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