Sensorcaine Injection, Solution
Product Images NDC 63323-461

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Sensorcaine (NDC 63323-461). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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 of SENSORCAINE active ingredient showing piperidine and aromatic ring with substituents, associated with hydrochloride and water molecules.*

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Chemical structure diagram depicting the molecular structure of the active ingredient in SENSORCAINE, showing a benzene ring with hydroxyl groups and an attached side chain containing a nitrogen atom.*

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SENSORCAINE (Bupivacaine HCl and Epinephrine Injection, USP) labeled with 0.25% concentration, equivalent to 125 mg per 50 mL (2.5 mg per mL). This 50 mL multiple dose vial is for infiltration and nerve block only, not for caudal, epidural, or spinal anesthesia. The label includes a warning about sulfites. Rx only.*

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Packaging label for SENSORCAINE (Bupivacaine HCl and Epinephrine Injection, USP) 0.25%, 125 mg per 50 mL (2.5 mg per mL) by APP Pharmaceuticals, LLC. The label states it is for infiltration and nerve block only and not for caudal, epidural, or spinal anesthesia. It contains epinephrine 1:200,000, with warnings about containing sulfites. The vial size is 25 multiple dose vials, 50 mL each. Additional storage and usage instructions are also included.*

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Label for SENSORCAINE 0.5% (Bupivacaine HCl and Epinephrine Injection, USP) containing epinephrine 1:200,000 as bitartrate. The label indicates 250 mg per 50 mL (5 mg per mL) in a 50 mL multiple dose vial by APP Pharmaceuticals, LLC. It is designated for nerve block only, with warnings against use for caudal, epidural, or spinal anesthesia and contains sulfites.*

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Sensorcaine 0.5% (Bupivacaine HCl and Epinephrine Injection, USP) multiple dose vial label. Contains 250 mg per 50 mL (5 mg/mL) with Epinephrine 1:200,000. For nerve block only, not for caudal, epidural, or spinal anesthesia. Contains sodium metabisulfite. Comes in 25 multiple dose vials of 50 mL each, labeled by APP Pharmaceuticals, LLC with storage and handling instructions.*

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Label for Sensorcaine-MPF injection by APP Pharmaceuticals, LLC, containing Bupivacaine HCl and Epinephrine USP. Strength is 0.25% (75 mg per 30 mL, 2.5 mg per mL) with Epinephrine 1:200,000 (as bitartrate). The 30 mL single-dose vial is indicated for infiltration, nerve block, caudal, and epidural anesthesia, not for spinal anesthesia. Methylparaben free, contains sulfites, Rx only.*

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Label for Sensorcaine-MPF injection by APP Pharmaceuticals, LLC, containing Bupivacaine HCl and Epinephrine (as bitartrate). The strength is 0.25% (2.5 mg/mL), with 75 mg per 30 mL vial. The label indicates use for infiltration, nerve block, caudal, and epidural anesthesia, warns of sulfite content, and states methylparaben free. It includes storage instructions and warnings for single-dose vials.*

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SENSORCAINE - MPF label for Bupivacaine HCl Injection, USP, 0.75% strength, providing 225 mg per 30 mL (7.5 mg per mL). It is intended for epidural and retrobulbar anesthesia, not for obstetric or spinal anesthesia. The label states it is methylparaben free and the vial size is 30 mL, single dose.*

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Packaging label for Sensorcaine-MPF (Bupivacaine HCl Injection, USP) 0.75% strength, containing 225 mg per 30 mL (7.5 mg per mL). The label states it is methylparaben free and intended for epidural and retrobulbar anesthesia, not for obstetric or spinal anesthesia. The package includes 25 single-dose vials of 30 mL each and is labeled for Rx only. Manufactured by APP Pharmaceuticals, LLC under Fresenius Kabi USA, LLC.*

* 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.