Lidocaine Hydrochloride Jelly
Product Images NDC 51662-1551

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Lidocaine Hydrochloride (NDC 51662-1551). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Urojet Labeling (51662 1551 2 Urojet Labeling)

Urojet Labeling (51662 1551 2 Urojet Labeling)
Lidocaine Hydrochloride Jelly, USP is a 2% solution available in a 20 mL dose. It contains 400 mg (20 mg/mL) of lidocaine hydrochloride for topical use. The product is manufactured by International Medication Systems, Limited in South El Monte, California. The item code is 3015-5P and the stock number is 76328-3015-5.*
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Case Labeling (51662 1551 3 Case Labeling)

Case Labeling (51662 1551 3 Case Labeling)
Lidocaine Hydrochloride Jelly is a local anesthetic used for topical use only. It has a usual dosage as per instructions given in the insert. The jelly is available in a 20mL URO-JET box of 25 with no preservative added, and should be stored at a controlled temperature of 15° to 30°C (59° to 86°F). The packaging should not be opened until ready to use. The syringe assembly requires aseptic technique and should not be assembled until ready for use. The manufacturer's package insert should be referred to for further information. The Original manufacturer's NDC is 76329-3015-5. This product is available only with a valid prescription.*
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Description (Description)

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Hs1 (How Supplied 1)

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Hs2 (How Supplied 2)

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Hs3 (How Supplied 3)

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Pouch Labeling (Pouch Labeling)

Pouch Labeling (Pouch Labeling)
The text describes a product called Lidocaine Hydrochloride Jelly USP, used as a local anesthetic for topical use only. The package contains one single-use syringe assembly, with no preservative added. The product should be stored at controlled room temperature between 15°C to 30°C. The manufacturer's package insert should be consulted before use. The product is available by prescription only and manufactured by HF Acquisition Co., LLC in Mukilteo, WA 98275.*
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Serialized Labeling (Serialized Labeling)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.