Flurbiprofen Sodium Solution/ Drops
Product Images NDC 63187-937

3 FDA label images from Proficient Rx Lp · 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 Flurbiprofen Sodium (NDC 63187-937). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

Symbol (8d90b181 36aa 4c80 8e43 Ba6239d07c8e 02)

Symbol (8d90b181 36aa 4c80 8e43 Ba6239d07c8e 02)
Flurbiprofen Sodium 0.3 mg/mL ophthalmic solution/drops packaged in a white carton. The box displays the product name, strength, dosage form, and route of administration. The labeler, Proficient Rx LP, is also shown on the packaging.*
FDA Label Image

63187-937-25 (Carton)

63187-937-25 (Carton)
Label for Flurbiprofen Sodium 0.03% ophthalmic solution, 2.5 mL, relabeled by Proficient Rx LP. The label states the product is for ophthalmic use only, includes the product ID RF093725, and storage conditions (15°-25°C). Originally manufactured by Bausch & Lomb Incorporated, Tampa, FL. Contains small repeated labels with lot, expiration, and NDC information.*
FDA Label Image

Chemstructure.jpg (Chemstructure)

Chemstructure.jpg (Chemstructure)
Chemical structure of flurbiprofen sodium dihydrate, showing the arrangement of aromatic rings, a fluorine atom, a methyl group, and the sodium carboxylate moiety with two water molecules of hydration.*

* 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.