Fluorescein Injection
Product Images NDC 51662-1533

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Fluorescein (NDC 51662-1533). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Vial (1533 2 Ak Fluor Vial Label)

Vial (1533 2 Ak Fluor Vial Label)
AK-FLUOR®10% is Fluorescein Injection that comes in a 5mL sterile vial with 100mg/mL concentration. It is meant for intravenous injection and has an NDC code of 17478-253-10. The rest of the text seems to be random numbers, letters, and symbols, not providing useful information.*
FDA Label Image

Pouch Label (1533 2 Pouch Label)

Pouch Label (1533 2 Pouch Label)
AK-FLUOR® 10% FLUORESCEIN INJECTION, USP is a sterile vial containing 100mg/mL of 5mL Fluorescein for IV injection. The usual dosage is available in the package insert. It should be stored at 20° to 25°C (68° to 77°F) and protected from freezing. It's only for diagnostic use. The manufacturer is HF Acquisition Co., LLC based in Mukilteo, WA 98275.*
FDA Label Image

Serialized Label (1533 3 Serialized Label)

FDA Label Image

Box Label (51662 1533 3 Hf Case Label Update)

Box Label (51662 1533 3 Hf Case Label Update)
AK-FLUOR® 10% Fluorescein Injection is a sterile vial used for IV injection for diagnostic purposes. It contains 100mg/mL of Fluorescein and comes in a package of 12 with a 5mL vial size. The usual dosage must be checked through the package insert. The storage temperature range is 20° to 25°C and it must be protected from freezing. The drug should only be used for diagnostic purposes. The product was manufactured by HF Acquisition Co., LLC and the original NDC was 17478-253-10. The expiration date of the product is January 1, 2030.*
FDA Label Image

Structure (Structure)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.