Naphcon A Solution/ Drops
Product Images NDC 0065-0085

7 FDA label images from Alcon Laboratories, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Naphcon A (NDC 0065-0085). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alcon Laboratories, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

15 mL Immediate Container (bottle)

15 mL Immediate Container (bottle)
Naphcon A ophthalmic solution eye drops, labeled for eye allergy relief, containing naphazoline hydrochloride 0.025% and pheniramine maleate 0.3%. The sterile solution is provided in a 15 mL (0.5 FL OZ) bottle by Alcon Laboratories, Inc. Directions for use and warnings are included on the label. The label states it relieves itching and redness and is clinically proven.*
FDA Label Image

15 mL Outer Container (carton)

15 mL Outer Container (carton)
Naphcon A eye drops packaging label by Alcon Laboratories, Inc. Contains 15 mL (0.5 FL OZ) of ophthalmic solution with active ingredients naphazoline hydrochloride 0.025% and pheniramine maleate 0.3%. Label highlights relief of itching and redness from eye allergies. Includes drug facts with active ingredients, uses, warnings, directions, and storage instructions. Features barcode and company address in Fort Worth, TX.*
FDA Label Image

15 mL Carton (15mlcarton)

15 mL Carton (15mlcarton)
Naphcon A eye drops label showing a 15 mL (0.5 FL OZ) solution containing napazoline hydrochloride 0.025% and pheniramine maleate 0.3%. The packaging indicates it is an ophthalmic redness reliever and antihistamine eye drop by Alcon Laboratories, Inc., a Novartis company. Drug facts, directions, inactive ingredients, warnings, and tamper evident details are included.*
FDA Label Image

2x5 mL Outer Containre (carton)

2x5 mL Outer Containre (carton)
The image shows the packaging label for Naphcon A eye drops, an ophthalmic solution by Alcon Laboratories, Inc. The label lists active ingredients as naphazoline hydrochloride 0.025% and pheniramine maleate 0.3%. It is for temporary relief of eye redness and itching. The package contains two 5 mL (0.17 FL OZ) bottles. Additional label information includes directions, warnings, inactive ingredients, storage instructions, and tamper-evident details.*
FDA Label Image

5 mL Immediate Container (bottle)

5 mL Immediate Container (bottle)
Naphcon A ophthalmic solution label showing active ingredients naphazoline hydrochloride 0.025% and pheniramine maleate 0.3%. The label states it is an eye allergy relief solution for redness and itching relief, sterile, 5mL (0.17 FL OZ). It includes directions, usage instructions, storage conditions, tamper-evident information, and the manufacturer Alcon Laboratories, Inc., Fort Worth, TX 76134 USA.*
FDA Label Image

5 mL Outercontainer (carton)

5 mL Outercontainer (carton)
Naphcon A eye drops packaging label displaying the product name, active ingredients naphazoline hydrochloride 0.025% and pheniramine maleate 0.3%, and its indication as redness reliever and antihistamine for temporary relief of itchy, red eyes. The label indicates a 5 mL (0.17 FL OZ) solution in a pocket-sized container by Alcon Laboratories, Inc., including usage directions, warnings, and storage instructions.*
FDA Label Image

Label

Label
Naphcon A ophthalmic solution eye drops label featuring active ingredients naphazoline hydrochloride 0.025% and pheniramine maleate 0.3% for eye allergy relief. The sterile 15 mL (0.5 fl oz) bottle is produced by Alcon Laboratories, Inc. The label highlights redness reliever and antihistamine properties and includes usage directions, warnings, and tamper-evident information.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.