Disposable Convenience Kit (single Shot Epidural)
Product Images NDC 69938-153

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Disposable Convenience Kit (single Shot Epidural) (NDC 69938-153). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by True Fit Rx 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

2b096527 4792 5c4c E054 00144ff88e88

This appears to be a product description for a Disposable Convenience Kit for a single-shot epidural tray. The brand name is TrueFit and the reorder number is 3105015. However, there is not enough information to provide a comprehensive description of the product.*

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Aplicare Povidone Iodine Pdp (Aplicare Povidone Iodine Pdp)

This is a drug solution with povidone-iodine as an active ingredient, used as an antiseptic. It comes in a sterile solution, packaged in a 0.75 fluid ounce container or 225 mL. The drug facts, including reorder number L-3001 and information on the active ingredient, are also provided. The remaining text seems to consist of gibberish.*

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Bupivacaine Pdp (Bupivacaine Pdp)

This is a single-dose medication containing 30mL of Bupivacaine. Each milliliter of the medication also contains other ingredients such as sodium chloride and may have pH adjusters. It is a sterile, nonpyrogenic solution with a concentration of 0.25%. The usual dosage and administration route should be obtained from the manufacturer's inert. It must be stored within a temperature range of 20-25°C. This medication cannot be used for spinal anesthesia. The manufacturer of this medication is Hospira, Inc. and the product code is RL-0342.*

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Lidocaine Pack Label (Lidocaine Pack Label)

This is a description of Hospira's Lidocaine HCI Injection, USP. The label indicates that this medication comes in a 5 mL package that is preservative-free. The lot number is 931153a, and the medication is set to expire on 1st September 2013. The manufacturer is Hospira Inc., based in Lake Forest, Illinois. The text also contains a reference to RL- 1467 which could be an internal code for the product.*

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Principal Display Panel (Principal Display Panel)

This is a description of a disposable convenience kit called TrueFit, designed for a single shot epidural tray. A reorder number is provided as 3105015. The has also captured the letter "B" which doesn't appear to be part of any relevant information.*

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Sodium Chloride 1 (Sodium Chloride 1)

This is a description of a pharmaceutical product. It is an ampule of Sodium Chloride solution with a concentration of 0.9% and 0.308 milliosmols per mL. The product is preservative-free and should be stored at a temperature between 15°-30°C. The manufacturer of the product is K.M. Pharm. Co., Ltd located in Jecheon, Korea 390-250, while it has manufactured for Spectra Medical Devices, Inc. located in Wilmington, MA 01887. The description also includes a LOT number and an expiration date (MM/YYYY).*

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Sodium Chloride 2 (Sodium Chloride 2)

This is a box of 25 ampuls of Sodium Chloride Injection, USP with a volume of SmL and NDC code 65262-1505-1. The solution has 0.9% concentration and is preservative-free. It is used for room temperature and cold ampersur at 15°C to 30°C. The product is manufactured by KA PHARM CO, LTD in Seoul, Korea and is distributed by SPECTRA MEDICAL DEVICES, INC in Wilmington, MA.*

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Bupivacaine Hydrochloride 1 (Bupivacaine Hydrochloride 1)

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Bupivacaine Hydrochloride 2 (Bupivacaine Hydrochloride 2)

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Lidocaine Hydrochloride Injection Figure 1 (Lidocaine Hydrochloride Injection Figure 1)

* 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.