Regenecare Ha Gel
Product Images NDC 66977-117

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Regenecare Ha (NDC 66977-117). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

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FDA Label Image

005670 Mp00117 R0720 V2

005670 Mp00117 R0720 V2
Regenecare is a topical anesthetic hydrogel in a spray form that contains Lidocaine HCI 2%. It provides temporary relief for pain and itching caused by minor burns, sunburn, small cuts, scrapes, insect bites, or minor skin irritations. The bottle should be shaken well before use, and it is available in a 4 fluid ounce (120 mL) size. The drug facts declare that Lidocaine HCI 2% is the active ingredient, which provides temporary relief as an anesthetic. It is only for external use and should be kept afar from children. Eye contact should be avoided, and medical assistance should be sought if the product is swallowed. If the symptoms remain persistently for over seven days or recur within a few days, the product shouldn't be used any more, and a doctor should be consulted. It is recommended to apply the product no more than 3 to 4 times a day for adults and children over two and consult a physician prior to prescribing the medication to children under two. It is advised to store the product at room temperature, avoid excessive heat, and not to freeze it. Other inactive ingredients include Aloe vera barbadensis leaf extract, Benzethonium chloride, Carbomer, Glycerin, lodopropynyl butylcarbamate, Procollagen, Sodium hyaluronate, Triethanolamine, Water. The product is manufactured for MPM Medical and available at www.mpmmed.com, with a reorder number of MP00117, and R0720.*

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