Bromsite Solution/ Drops
Product Images NDC 49708-754

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Bromsite (NDC 49708-754). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Spl-bromsite-str (Spl Bromsite Str)

Chemical structure of bromfenac, the active ingredient in BROMSITE 0.075% ophthalmic solution, showing aromatic rings including a bromine atom, an amino group, a carboxylate sodium salt, and a hydrate molecule (1.5 water).*

FDA Label Image

Spl-bromsite-fig A (Spl Bromsite Figa)

An instructional illustration showing a hand holding a small dropper bottle with the other hand positioned to receive drops from the bottle. The image depicts the proper way to use ophthalmic solution drops, likely representing BROMSITE 0.075% bromfenac ophthalmic solution.*

FDA Label Image

Spl-bromsite-fig B (Spl Bromsite Figb)

An instructional illustration labeled "Figure B" showing a hand holding an eye drop bottle while the other hand removes the protective cap by twisting it off. The image demonstrates how to open the ophthalmic solution bottle for BROMSITE 0.075% (bromfenac) eye drops.*

FDA Label Image

Spl-bromsite-fig C (Spl Bromsite Figc)

An instructional illustration labeled Figure C shows a hand tilted with the palm up and fingers slightly curved, demonstrating the motion of turning or rotating an object with the thumb and index finger. No text beside the image clarifies the specific action.*

FDA Label Image

Spl-bromsite-fig D (Spl Bromsite Figd)

An instructional illustration showing the proper method to invert the hand with the medication bottle, likely to aid in dispensing ophthalmic solution drops. The image depicts one hand holding the bottle upside down above the other hand, which is facing upward.*

FDA Label Image

Spl-bromsite-fig E (Spl Bromsite Fige)

An instructional line drawing labeled Figure E showing one hand holding an ophthalmic dropper bottle upside down above the fingers of the other hand, depicting the proper technique for instilling eye drops.*

FDA Label Image

Spl-bromsite-fig F (Spl Bromsite Figf)

An instructional illustration showing a person administering ophthalmic solution drops to the eye, demonstrating the proper method of using eye drops by tilting the head back and placing drops into the open eye.*

FDA Label Image

Spl-bromsite-foil-label (Spl Bromsite Foil Label)

The image shows the packaging label for BROMSITE 0.075% (bromfenac ophthalmic solution) in a 5 mL dosage form. The label displays the product name and strength repeatedly across the panel. It includes a barcode and instructions stating, "Do not use if foil pouch is open." The label is from Sun Pharmaceutical Industries, Inc., and specifies the ophthalmic route.*

FDA Label Image

Spl-bromsite-bottle-label (Spl Bromsite Bottle Label)

Label for BROMSITE 0.075% bromfenac ophthalmic solution containing 0.87 mg bromfenac sodium sesquihydrate per mL, equivalent to 0.76 mg bromfenac free acid. The label indicates a sterile 5 mL solution for ophthalmic use by prescription, distributed by Sun Pharmaceutical Industries, Inc., with NDC 49708-754-41.*

FDA Label Image

Spl-bromsite-carton-label (Spl Bromsite Carton Label)

Packaging label for BROMSITE 0.075% ophthalmic solution by Sun Pharmaceutical Industries, Inc. The label states bromfenac as the active ingredient at 0.76 mg/mL strength, supplied in a sterile 5 mL dropper bottle. The label includes directions for topical eye application and storage instructions. The product is Rx only and distributed by Sun Pharmaceutical Industries, Cranbury, NJ.*

* 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.