Glostrips Strip
Product Images NDC 51801-009

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Glostrips (NDC 51801-009). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nomax 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

Figure 1 (Glostrips01)

An instructional illustration depicting two hands pulling apart a strip or wrapper along a center line or perforation, labeled as Fig. 1. The image appears to demonstrate how to open or separate the packaging of the product, GloStrips Fluorescein Sodium ophthalmic strips.*

FDA Label Image

Figure 2 (Glostrips02)

An instructional diagram labeled Fig. 2 showing hands peeling or separating a small strip, likely demonstrating the proper method to handle or prepare a GloStrips fluorescein sodium ophthalmic strip for use.*

FDA Label Image

Figure 3 (Glostrips03)

An instructional line drawing labeled 'Fig. 3' showing two hands holding and pulling apart a strip, indicating separation of the ophthalmic strip product GloStrips containing Fluorescein Sodium.*

FDA Label Image

Figure 4 (Glostrips04)

An instructional line drawing labeled as Figure 4 illustrating a hand holding a small ophthalmic strip, consistent with the description of an ophthalmic fluorescein sodium strip device.*

FDA Label Image

Principal Display Panel (300 Strip Carton)

Label for GloStrips 1.0, fluorescein sodium ophthalmic strips containing 1.0 mg of active ingredient per strip. The label indicates 300 sterile strips per package and displays the manufacturer Amcon Laboratories, Inc. The product NDC is 51801-009-50.*

* 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.