Bromsite Solution/ Drops
Product Images NDC 49708-754

10 FDA label images from Sun Pharmaceutical Industries, Inc. · Packaging, Regulatory Labels, and Product Appearance

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

Bromfenac Chemical Structure (Bromsite 01)

Bromfenac Chemical Structure (Bromsite 01)
Chemical structure of bromfenac sodium sesquihydrate, the active ingredient in BROMSITE 0.075%, an ophthalmic solution.*
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Instructions For Use (Figure A)

Instructions For Use (Figure A)
An instructional illustration labeled as Figure A showing a person holding an ophthalmic drop bottle over an open palm. The image demonstrates positioning the bottle vertically to dispense drops into the palm, typically associated with eye drop administration guidance.*
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Instructions For Use (Figure B)

Instructions For Use (Figure B)
An illustration showing a hand holding an eye drop bottle with the other hand twisting the cap to open it, likely indicating how to prepare ophthalmic drops for use.*
FDA Label Image

Instructions For Use (Figure C)

Instructions For Use (Figure C)
Illustration showing a hand with a dropper positioned above the palm, demonstrating how to dispense ophthalmic solution drops into the palm by gently tilting the container.*
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Instructions For Use (Figure D)

Instructions For Use (Figure D)
An instructional diagram labeled Figure D shows a hand holding a small container and tipping it downward toward an open palm, demonstrating how to dispense drops into the palm of the hand, likely indicating how to handle or prepare bromfenac ophthalmic solution drops.*
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Instructions For Use (Figure E)

Instructions For Use (Figure E)
Instructional illustration showing a person holding an ophthalmic drop bottle inverted above the index finger of the opposite hand, presumably demonstrating how to administer eye drops.*
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Instructions For Use (Figure F)

Instructions For Use (Figure F)
Illustration showing a person administering ophthalmic drops by tilting the head back and applying drops into the eye from a dropper.*
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5 mL Foil Wrapper (Bromsite 08)

5 mL Foil Wrapper (Bromsite 08)
The packaging label for BROMSITE 0.075%, an ophthalmic solution containing bromfenac at 0.075% (.76 mg/mL) strength. The label indicates a 5 mL solution by Sun Pharmaceutical Industries, Inc., and includes text reminders about the lot number, expiration date, and instructions not to use if the foil pouch is open. The label is primarily blue with sections marked for barcode and artwork.*
FDA Label Image

5 mL Bottle Label (Bromsite 09)

5 mL Bottle Label (Bromsite 09)
Label for BROMSITE 0.075% bromfenac ophthalmic solution by Sun Pharmaceutical Industries, Inc. The label shows the active ingredient bromfenac sodium sesquihydrate equivalent to 0.76 mg/mL bromfenac free acid. It includes the NDC 49708-754-41, barcode, lot number AB12C34D, and expiration date 01/10. The label indicates the product is an ophthalmic solution in a drops dosage form.*
FDA Label Image

5 mL Carton Label (Bromsite 10)

5 mL Carton Label (Bromsite 10)
Packaging label for BROMSITE 0.075% (bromfenac ophthalmic solution) by Sun Pharmaceutical Industries, Inc. The label indicates a sterile 5 mL ophthalmic solution with 0.76 mg/mL strength. Instructions include topical eye application, dosage, storage conditions, and a note to discard after treatment completion. The label features the product name, active ingredient, and distribution details.*

* 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.