Product Images Bacitracin Zinc, Neomycin Sulfate And Polymyxin B Sulfate

This is a description of a medication product called Lidocaine Hydrochloride Jelly USP, 2%. It comes in a sterile 5 mL package with a NDC number of 17478-840-05. The jelly is indicated for use as a local anesthetic and is an aqueous solution of lidocaine hydrochloride, hypromeliose, methyl and propylparaben, sodium hydroxide, and/or hydrochloric acid. The dosage information is available in the package insert, and it should be stored at 20° to 25°C (68" to 77°F) and discarded if unused. This medication is for topical use only, and not for ophthalmic use. This drug should be kept out of the reach of children. The product is made by Akom, Inc. in Lake Forest, IL 60045.*

This appears to be a label for a post-operative system, possibly containing medication and staple removal tools. The product's NDC (National Drug Code) is 70529-941-01.*

The given text is a mix of alphanumeric characters and some sentences related to drug usage instruction, warning labels, and other product details. It seems like a description of a triple antibiotic ointment used for first-aid purposes to prevent infections in minor cuts, bites or burns. The text includes active ingredients, directions for use, and warnings against allergic reactions or over-usage. The product seems to have been manufactured in Israel and is distributed by Dynarex Corporation based in Orangeburg, NY.*