Carboxymethylcellulose Sodium 0.5% Solution/ Drops
Product Images NDC 51407-945

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Carboxymethylcellulose Sodium 0.5% (NDC 51407-945). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Golden State Medical Supply, 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

30ea Case (30ea Case (ek9046 00))

30ea Case (30ea Case (ek9046 00))
The image shows a packaging label for Carboxymethylcellulose Sodium 0.5% lubricant eye drops. It is a sterile ophthalmic solution supplied in 30 single-use containers of 0.02 FL OZ (0.5 mL) each. The label indicates the product is preservative-free and includes drug facts, warnings, directions, inactive ingredients, and manufacturer information. The labeler is listed as Golden State Medical Supply, Inc.*
FDA Label Image

Pe Label (Pe Label (el9044 00))

Pe Label (Pe Label (el9044 00))
Label for Carboxymethylcellulose Sodium Eye Drops Single-Use, indicating a volume of 0.5 mL per unit. The label includes placeholder manufacturing and expiration dates and features the Golden State Medical Supply (GSMS) logo along with a QR code. Dimensions of the label area are 25mm by 8mm.*
FDA Label Image

Pouch (Pouch (ei9018 00))

Pouch (Pouch (ei9018 00))
Label for Carboxymethylcellulose Sodium 0.5% Lubricant Eye Drops, preservative free, single-use 0.5 mL solution. The label features the product name prominently and includes instructions to open along the dotted line. It shows a barcode and the gsms trademark near the bottom. Manufacturer details are not fully visible.*

* 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.