Tetracaine Hydrochloride Solution
Product Images NDC 70069-597

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Tetracaine Hydrochloride (NDC 70069-597). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Somerset Therapeutics, Llc, 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

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Chemical structure diagram of Tetracaine Hydrochloride showing the molecular arrangement with functional groups including an aromatic ring, amino group, ester linkage, and hydrochloride salt moiety.*
FDA Label Image

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Label for Tetracaine Hydrochloride Ophthalmic Solution, USP 0.5%, 5 mL sterile solution for ophthalmic use. The label includes storage instructions (store at 15° to 25°C, protect from light), warnings about tamper evident seal, and manufacturer information for Somerset Therapeutics, LLC, Somerset, NJ. Made in India.*
FDA Label Image

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Label for Tetracaine Hydrochloride Ophthalmic Solution, USP 0.5% (5 mg/mL), 5 mL sterile solution for ophthalmic use. Manufactured for Somerset Therapeutics LLC. The label includes active, preservative, and inactive ingredients, storage instructions, and warnings. NDC 70069-596-01.*
FDA Label Image

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Label for Tetracaine Hydrochloride Ophthalmic Solution, USP 0.5% (5 mg/mL) in a 15 mL bottle. It is a sterile solution for ophthalmic use, manufactured by Somerset Therapeutics, LLC. The label includes active and inactive ingredient information, storage instructions, and a tamper-evident seal warning.*
FDA Label Image

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Image (8d8c6ec7 7369 4f34 88bf E8827fb87ef0 05)
Label for Tetracaine Hydrochloride Ophthalmic Solution, USP 0.5%, 15 mL sterile solution by Somerset Therapeutics, LLC. The label includes active ingredient strength, NDC 70069-597-01, preservative and inactive ingredients list, storage instructions, a warning to keep out of reach of children, and a statement to not use if the tamper-evident seal is broken.*

* 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.