Lasix Onyu Injection
Product Images NDC 81137-001

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 57 technical images submitted to the FDA as part of the official labeling for Lasix Onyu (NDC 81137-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sq Innovation, 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.

Product Images & Figures Index

FDA Label Image

Image-10 (Image 10 Step 2 Ru Charging)

Image-10 (Image 10 Step 2 Ru Charging)
An instructional illustration showing the setup of a medical device connected to a power adapter plugged into an electrical outlet. The image includes two close-up views of the device with indicator icons: one displays a green checkmark with a solid blue symbol, and the other shows a blue blinking light, likely indicating device status or operation modes.*
FDA Label Image

Image-11 (Image 11 Step 3 Hand Washing)

Image-11 (Image 11 Step 3 Hand Washing)
Black and white line drawing showing a person washing hands under a water faucet, with water flowing over the hands into a sink. The illustration emphasizes hand hygiene.*
FDA Label Image

Image-12 (Image 12 Step 4 Kit Back Lot Exp)

Image-12 (Image 12 Step 4 Kit Back Lot Exp)
LASIX ONYU furosemide 30 mg/mL injection in a subcutaneous route is shown in its packaging box. The label includes dosing and storage instructions, a barcode, serial number, expiration date placeholder, and lot number. The product is labeled by SQ Innovation, Inc., Burlington, MA, USA, with NDC 81137-001.*
FDA Label Image

Image-12.5 (Image 12.5 Step 5 Treatment Kit Contents)

Image-12.5 (Image 12.5 Step 5 Treatment Kit Contents)
LASIX ONYU 30 mg/mL furosemide injection for subcutaneous use by SQ Innovation, Inc. The image shows alcohol pad packets, a single-dose prefilled cartridge box, and a sealed disposable unit package. The prefilled cartridge packaging highlights the product's strength and route of administration.*
FDA Label Image

Image-13 (Image 13 Step 6 Cartridge Du)

Image-13 (Image 13 Step 6 Cartridge Du)
Illustration showing components of a subcutaneous injection system for LASIX ONYU (furosemide) including a prefilled cartridge with a silver top, a disposable unit with adhesive and a paper liner, and two alcohol pads.*
FDA Label Image

Image-14 (Image 14 Step 7 Cartridge Hand)

Image-14 (Image 14 Step 7 Cartridge Hand)
An instructional illustration showing a hand holding a vial with a silver top. The silver top is labeled with an arrow pointing to it, indicating a focus on the vial's cap, relevant for the preparation or use of an injectable drug.*
FDA Label Image

Image-15 (Image 15 Step 8 Wipe Tube Alcohol)

Image-15 (Image 15 Step 8 Wipe Tube Alcohol)
An instructional illustration depicting a hand holding a small vial with a silver top, demonstrating preparation for injection. To the right, there is a small packet labeled 'ALCOHOL PAD,' indicating cleaning before injection.*
FDA Label Image

Image-16 (Image 16 Step 9 Du Drug Cartridge Blue Arrow Together)

Image-16 (Image 16 Step 9 Du Drug Cartridge Blue Arrow Together)
An instructional illustration showing two steps of inserting an injection cartridge into a device. The first step shows pushing the cartridge with a silver top into the device, and the second step shows the cartridge securely positioned inside the device, guided by blue arrows indicating the direction of insertion.*
FDA Label Image

Image-17 (Image 17 Step 10 Infusor Slide Together)

Image-17 (Image 17 Step 10 Infusor Slide Together)
An instructional illustration showing hands holding a device that consists of a reusable unit and a disposable unit, labeled respectively. The diagram also identifies a battery light and a status light on the reusable unit, highlighting key components and indicators of the device.*
FDA Label Image

Image-18 (Image 18 Step 11 Ru Status)

Image-18 (Image 18 Step 11 Ru Status)
An instructional diagram depicting three different states of a device indicator light and corresponding audio tones. The first shows a blue flashing light with an OK tone of one long beep and a green check mark. The second shows a red flashing light with an alarm tone of two short beeps and a red X mark. The third shows a solid red battery icon with no tone and a red X mark. The image illustrates device status signals related to battery or operation conditions.*
FDA Label Image

Image-19 (Image 19 Step 12 Infusor Placement)

Image-19 (Image 19 Step 12 Infusor Placement)
An instructional diagram showing two possible subcutaneous injection sites on the abdomen for LASIX ONYU (furosemide) injection. The image presents two areas on the lower abdomen where the injection can be administered, indicated with arrows and the word 'Or' between them.*
FDA Label Image

Image-20 (Image 20 Step 13 Wipe Abdomen Alcohol Pad)

Image-20 (Image 20 Step 13 Wipe Abdomen Alcohol Pad)
An illustration showing a person cleaning the skin on their abdomen with an alcohol pad, preparing the injection site for subcutaneous administration. The alcohol pad is labeled."*
FDA Label Image

Image-21 (Image 21 Step 14 Du Peel Liner Detail)

Image-21 (Image 21 Step 14 Du Peel Liner Detail)
An instructional illustration showing hands peeling a paper liner from an adhesive-backed medical device component. The image highlights the adhesive area under the peeled back paper liner tab, with a close-up inset emphasizing the peeling action.*
FDA Label Image

Image-22 (Image 22 Step 15 Infusor Press Button Lights Up Detail)

Image-22 (Image 22 Step 15 Infusor Press Button Lights Up Detail)
An instructional illustration showing a hand holding a small rectangular device with a status light and start/stop button facing up. The device is being positioned for subcutaneous injection on the abdominal area above the belt line. A close-up inset highlights the status light and button on the device's top face.*
FDA Label Image

Image-23 (Image 23 Step 16 Infusor Smooth Adhesive Edge)

Image-23 (Image 23 Step 16 Infusor Smooth Adhesive Edge)
An instructional illustration showing a person applying a medical patch device to the lower abdomen area. The person’s hands are positioned around the patch, which appears to be an infusion or injection device, attached on the skin above the belt line. The image visually demonstrates the placement of a subcutaneous drug delivery device.*
FDA Label Image

Image-24 (Image 24 Step 17 Infusor Press Button)

Image-24 (Image 24 Step 17 Infusor Press Button)
An instructional illustration showing a person applying a subcutaneous injection device to their abdomen. A close-up highlights the device, labeled with the word 'Slow,' indicating a slow release or delivery mechanism for the medication.*
FDA Label Image

Image-25 (Image 25 Step 18 Ru Check Status2)

Image-25 (Image 25 Step 18 Ru Check Status2)
Illustration depicting a device with two indicator lights and corresponding audio tones. The top panel shows a green check mark, a slow blinking blue light, and an OK Tone represented by one long beep. The bottom panel shows a red X, a constantly lit red light, and an Alarm Tone represented by two short beeps.*
FDA Label Image

Image-26 (Image 26 Step 19 Time Wait 5 Hours)

Image-26 (Image 26 Step 19 Time Wait 5 Hours)
An instructional illustration of a clock face showing the time 12:25 with a shaded segment indicating a waiting period, accompanied by the text 'Wait 5 Hours' below the clock.*
FDA Label Image

Image-27 (Image 27 Step 20 Ru Status 3)

Image-27 (Image 27 Step 20 Ru Status 3)
An instructional diagram showing three device status indicators for a subcutaneous injection system. The top panel shows a green check mark beside a blue solid circle and a single long beep tone indicating OK status. The middle panel shows a red X with a red flashing light and two short beeps indicating an alarm status. The bottom panel shows a green check mark beside a slowly flashing blue light with one long beep for OK status.*
FDA Label Image

Image-28 (Image 28 Step 21 Infusor Peel Away Abdomen)

Image-28 (Image 28 Step 21 Infusor Peel Away Abdomen)
An instructional illustration showing a wearable drug delivery device attached to a person's abdominal area, secured by a belt. A blue arrow points toward the device, indicating an action related to device use or placement.*
FDA Label Image

Image-29 (Image 29 Step 22 Confirmation Infusion Worked)

Image-29 (Image 29 Step 22 Confirmation Infusion Worked)
Illustration showing the back of an infusor device with a close-up of a window containing a gray stopper. It compares correct placement of the gray stopper in the middle of the window (marked with a green check) to two incorrect configurations with air bubbles and stopper misalignment (both marked with red X).*
FDA Label Image

Image-3 (Image 3 Infusor Blue Status Blue Tab)

Image-3 (Image 3 Infusor Blue Status Blue Tab)
Illustration of a handheld medical device likely used for subcutaneous injection with an indicator light, button, and battery symbol visible. The device has a two-tone design with white and light green sections and appears to be designed for user interaction.*
FDA Label Image

Image-30 (Image 30 Step 23 Toilet)

FDA Label Image

Image-31 (Image 31 Step 24 Infusor Slide Apart)

Image-31 (Image 31 Step 24 Infusor Slide Apart)
Illustration showing hands separating a device into two parts labeled 'Reusable Unit' and 'Disposable Unit.' The disposable unit is being pulled away from the reusable unit, with arrows indicating the direction of separation.*
FDA Label Image

Image-32 (Image 32 Step 25 Du Sharps Disposal)

Image-32 (Image 32 Step 25 Du Sharps Disposal)
An instructional illustration shows a hand holding a prefilled syringe or injection device positioned above a sharps disposal container labeled "SHARPS DISPOSAL." The syringe is oriented to be safely deposited into the container, emphasizing proper disposal of medical sharps.*
FDA Label Image

Image-33 (Image 33 Step 26 Ru Wipe Off)

Image-33 (Image 33 Step 26 Ru Wipe Off)
An instructional line drawing showing hands cleaning a small medical device with a cloth or wipe. The device has a battery indicator and a socket port, indicating it is an electronic injection or infusion device, possibly related to subcutaneous administration.*
FDA Label Image

Image-34 (Image 34 Step 27 Starter Kit Storage)

Image-34 (Image 34 Step 27 Starter Kit Storage)
Packaging label of LASIX ONYU Starter Kit by SQ Innovation, Inc., containing furosemide injection 30 mg/mL for subcutaneous use. The box is marked as a starter kit with multiple components indicated inside, showing the product name, strength, dosage form, and labeler information.*
FDA Label Image

Image-35 (Image 35 Fda Sharps Qr Code)

Image-35 (Image 35 Fda Sharps Qr Code)
Text panel containing detailed prescribing information and drug facts for LASIX ONYU (furosemide) injection, 30 mg/mL. The panel includes sections on indications, dosage, administration, contraindications, warnings, adverse reactions, and storage instructions, consistent with FDA labeling requirements for a human prescription subcutaneous injection product by SQ Innovation, Inc.*
FDA Label Image

Image-36 (Image 36 Lights Tones Table)

Image-36 (Image 36 Lights Tones Table)
Diagram showing status light and tone indicators for an infusion device. It illustrates different battery light colors and flashing patterns (blue, red) and status light behaviors, with corresponding tones (no tone, OK tone, alarm tone) and meanings related to battery charging, readiness, medicine delivery, and error conditions.*
FDA Label Image

Image-37 (Image 37 Ru Battery Blue Blinking)

Image-37 (Image 37 Ru Battery Blue Blinking)
An instructional or technical illustration depicting a device with a highlighted button, likely for activation or indication, showing a blue illuminated symbol resembling a capsule or pill. The image includes mechanical details such as a circular component and grooves, suggesting a medical device interface, without textual information or branding.*
FDA Label Image

Image-38 (Image 38 Ru Battery Blue)

Image-38 (Image 38 Ru Battery Blue)
An illustration showing a device likely used for subcutaneous injection administration. The device has a blue charging or status indicator, a circular button or dial, and a defined compartment area, suggesting it is designed for controlled delivery of medication such as LASIX ONYU injection.*
FDA Label Image

Image-39 (Image 39 Ru Battery Red)

Image-39 (Image 39 Ru Battery Red)
An illustration showing a medical injection device, likely designed for subcutaneous administration. The device is white with a red indicator and features a circular component on one end, presumably the injection button or needle cover. The design appears to be a pen-style injector suitable for delivering medication doses.*
FDA Label Image

Image-40 (Image 40 Infusor Battery Red Blue Tab)

Image-40 (Image 40 Infusor Battery Red Blue Tab)
An illustration showing a subcutaneous injection device with a partly transparent cover, highlighting the internal component that holds a small vial or cartridge. The device features a button and indicator lights, likely used to administer an injection dose.*
FDA Label Image

Image-41 (Image 41 Ru Battery Red Status)

Image-41 (Image 41 Ru Battery Red Status)
An illustration diagram of a subcutaneous injection device, likely used for administering LASIX ONYU (furosemide) injection 30 mg/mL by SQ Innovation, Inc. It shows a rectangular handheld device with a button, indicator light, and injection area, designed for patient self-administration.*
FDA Label Image

Image-42 (Image 42 Infusor Status Blinking Red Body)

Image-42 (Image 42 Infusor Status Blinking Red Body)
Illustration showing a wearable drug delivery device with a subcutaneous injection site. The image displays the device detached and attached to the skin on the abdomen, indicating its proper placement. The device features indicator lights and a button, commonly used for subcutaneous administration of medications like LASIX ONYU (furosemide) injection.*
FDA Label Image

Image-43 (Image 43 Ru Alarm Red)

Image-43 (Image 43 Ru Alarm Red)
Illustration showing a device with a low battery icon, a red flashing indicator light, and a circular button. Below the device, a speaker icon indicates an alarm tone described as "2 short beeps." This diagram likely represents a device alert for low battery or an alarm signal.*
FDA Label Image

Image-44 (Image 44 Infusor Status Blinking Red Body Alarm)

Image-44 (Image 44 Infusor Status Blinking Red Body Alarm)
An instructional illustration showing a subcutaneous injection device for LASIX ONYU furosemide 30 mg/mL. The image includes two views: a close-up of the device with a battery indicator and a red alert light, and the device worn on a person's waist, secured by a belt. An alarm tone symbol indicating two short beeps is also depicted, suggesting an alert feature of the device.*
FDA Label Image

Image-44.5 (Image 44.5 Press Hold Start Stop Button)

Image-44.5 (Image 44.5 Press Hold Start Stop Button)
An instructional illustration showing a hand holding a device applied to the lower abdominal area of a person, indicating subcutaneous injection or administration technique. The image highlights the placement of the device just above the waistline.*
FDA Label Image

Image-45 (Image 45 Status Light Flashing Red Blue)

Image-45 (Image 45 Status Light Flashing Red Blue)
An illustration showing two subcutaneous infusion pump units. The top pump displays a green check mark and a red alarm light with a label indicating an alarm tone of 2 short beeps. The bottom pump shows a red X, a blue light labeled 'Slow,' indicating an incorrect or undesired state.*
FDA Label Image

Image-46 (Image 46 Toilet)

FDA Label Image

Image-47 (Image 47 Confirmation Infusion Worked)

Image-47 (Image 47 Confirmation Infusion Worked)
An instructional illustration showing the back of an infusor device with a close-up of the syringe window. It indicates a correct placement with a gray stopper in the middle of the window marked by a green check, and two incorrect placements where the gray stopper is absent and an air bubble is visible, each marked with a red X.*
FDA Label Image

Image-48 (Image 48 Ru Infusor No Lights)

Image-48 (Image 48 Ru Infusor No Lights)
An instructional diagram depicting two views of a medical injection device. The device has a rectangular body with a battery icon, a circular button, and a textured grip area. The lower view shows the device with a protective cover or overlay highlighted in green, illustrating assembly or usage steps.*
FDA Label Image

Image-49 (Image 49 Ru Charging Status)

Image-49 (Image 49 Ru Charging Status)
An illustration showing two views of an electronic device with a battery icon indicator and a circular control button. Also included is a separate image of a power adapter with a coiled cable, featuring a USB connector. The device and charger appear to be related components, likely for use with a medication delivery system or injection device.*
FDA Label Image

Image-5 (Image 5 Kit Contents Horizontal Text)

Image-5 (Image 5 Kit Contents Horizontal Text)
Packaging items for LASIX ONYU 30 mg/mL subcutaneous injection by SQ Innovation, Inc. The image shows two separate alcohol pad packets, a disposable unit packet labeled for single use only, and a carton for single-dose prefilled cartridges. All items are labeled consistent with this product and intended for injection preparation and administration.*
FDA Label Image

Image-50 (Image 50 Assembled Device Off)

Image-50 (Image 50 Assembled Device Off)
Illustration showing a single-use subcutaneous injection device for LASIX ONYU (furosemide) 30 mg/mL injection. The device includes visual indicators such as a battery symbol and a central button or dial, designed for patient self-administration.*
FDA Label Image

Image-51 (Image 51 Infusor Ready)

Image-51 (Image 51 Infusor Ready)
An instructional illustration showing a subcutaneous injection device for LASIX ONYU (furosemide) 30 mg/mL. It displays two states: a ‘Fast’ setting indicated by a blue light and one long beep labeled as OK Tone, and an alert state with a red light and two short beeps labeled as Alarm Tone.*
FDA Label Image

Image-52 (Image 52 Symbols Legend)

Image-52 (Image 52 Symbols Legend)
A symbol legend table explaining various symbols used on medical device or pharmaceutical packaging. It includes warnings, prescription use, handling instructions like "Keep dry" and "Do not use if package is damaged," technical symbols for equipment operation, and indicators for single use or reusable units. Symbols such as manufacturer, date of manufacture, serial number, and sterilization method are also defined.*
FDA Label Image

Image-6 (Image 6 Ru Charger)

Image-6 (Image 6 Ru Charger)
An illustration showing two components labeled as Reusable Unit and Charger. The Reusable Unit appears to be a handheld device with a button and circular feature, while the Charger consists of a power plug with a coiled cord ending in a connector.*
FDA Label Image

Image-7 (Image 7 Starter Kit)

Image-7 (Image 7 Starter Kit)
Packaging labels for LASIX ONYU injection, furosemide 30 mg/mL by SQ Innovation, Inc. The image shows a Starter Kit box, three individual Lasix ONYU Kits, an Instructions for Use leaflet, and a Reusable Unit and Charger Box. The product is for subcutaneous administration.*
FDA Label Image

Image-8 (Image 8 Get To Know Infusor Parts)

Image-8 (Image 8 Get To Know Infusor Parts)
An instructional diagram showing components of a medical device including a charger and two units: disposable and reusable. The disposable unit has labeled cartridge port, adhesive (front), paper liner, needle hole, and window to view stopper (back). The reusable unit shows status light, start/stop button, battery light (front), and charger insertion point (back).*
FDA Label Image

Image-9 (Image 9 Step 1 Ru Charger Kit)

Image-9 (Image 9 Step 1 Ru Charger Kit)
Packaging for LASIX ONYU injection, a subcutaneous furosemide product at 30 mg/mL by SQ Innovation, Inc. The image shows a reusable unit device, an electrical charger with cord and plug, and the LASIX ONYU Kit box featuring the product name and instructions to lift and open.*
FDA Label Image
FDA Label Image

Starter-kit (Starter Kit Label)

Starter-kit (Starter Kit Label)
Packaging label for LASIX ONYU (furosemide injection) 30 mg/mL, a subcutaneous injection by SQ Innovation, Inc. The label identifies this product as a sterile, single-use solution without preservatives and indicates it is a Starter Kit including a reusable unit, charger, Lasix ONYU kits, and instructions for use. The label is designed for the 30 mg/mL strength and specifies single-dose prefilled cartridge use.*
FDA Label Image

Image-structure (Structure)

Image-structure (Structure)
Chemical structure diagram of furosemide showing its molecular framework with labeled functional groups including a carboxyl group, sulfonamide, chlorine atom, and furan ring.*
FDA Label Image

Image-training (Training Video)

Image-training (Training Video)
A training video information panel featuring a QR code and a website URL for www.Lasix-ONYU.com/infusor-training, intended for accessing training materials related to LASIX ONYU injection.*
FDA Label Image

Treatment-kit (Treatment Kit Label)

Treatment-kit (Treatment Kit Label)
Packaging label for Lasix ONYU injection, furosemide 80 mg/2.67 mL (30 mg/mL) for subcutaneous use. The label details that it is a single-use, sterile solution with no preservatives. The box contains a single-dose prefilled cartridge, a disposable unit, and two alcohol pads. Labeler is SQ Innovation, Inc.*
FDA Label Image

Image-warning (Warning)

Image-warning (Warning)
A warning text panel for LASIX ONYU Injection (furosemide) emphasizing not to use insulin or other medicine cartridges in the Lasix ONYU Infusor due to the risk of severe injury. It advises using only the Lasix ONYU Prefilled Cartridge with the infusor device.*

* 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.