Fluorescite Injection, Solution
Product Images NDC 0065-0092

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Fluorescite (NDC 0065-0092). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alcon, 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

Carton (Carton)

Label for Fluorescite 10% (fluorescein sodium injection) sterile solution, 100 mg/mL strength. The label indicates 1 dozen 5 mL vials, intended for intravenous use, manufactured by Alcon Laboratories, Inc. Storage instructions specify 2° to 25° C and not to freeze. The label includes an NDC barcode and spaces for manufacturing and expiration dates.*

FDA Label Image

Carton (Carton2)

Packaging label for Fluorescite 10% (fluorescein injection, USP) 100 mg/mL solution for injection, sterile, for intravenous use. The label indicates it is Rx only, provided in a carton of 1 dozen 5 mL vials. The product is labeled by Alcon Laboratories, Inc., a Novartis company. Storage instructions specify 2° to 25° C and not to freeze.*

FDA Label Image

Chemical (Chemical)

Chemical structure of fluorescein sodium, the active ingredient in FLUORESCITE 100 mg/mL ophthalmic injection solution by Alcon, Inc. The structure shows aromatic rings with sodium carboxylate groups and ketone functions characteristic of fluorescein sodium.*

FDA Label Image

Label (Label)

Label for Fluorescite 10% (fluorescein injection, USP) 100 mg/mL sterile ophthalmic injection solution. The 5 mL vial label shows the product name, strength, volume, and manufacturer Alcon Laboratories, Inc., Fort Worth, Texas. Includes NDC 0065-0092-65 and spaces for lot number and expiration date.*

* 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.