Bio-scriptives Lidum
Product Images NDC 60608-011

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Bio-scriptives Lidum (NDC 60608-011). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Biochemics, 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.

FDA Label Image

Lidumback1 (Lidumback1)

Drug Facts panel for Bio-Scriptives Lidum showing active ingredient Lidocaine 5% as a topical anesthetic. It lists uses including rapid onset relief for minor burns, scrapes, sunburn, skin irritations, cuts, and insect bites. Warnings advise external use only and caution against use in or near eyes and over large raw or blistered areas. Instructions to stop use if allergic reactions occur or condition worsens or does not improve within 7 days are provided.*

FDA Label Image

Lidumback2 (Lidumback2)

Drug Facts label panel for Bio-Scriptives Lidum showing directions for use, stating that adults and children 2 years and older should apply externally to affected areas 3-4 times a day. It also lists inactive ingredients including Aloe Vera Juice, Water, Cholesterol, Isopropyl Myristate, and others. The panel includes a keep out of reach of children warning and distributor contact information for Bio-Scriptives.*

FDA Label Image

Lidumfront (Lidumfront)

Label for Bio-Scriptives Lidum topical anesthetic cream containing 5% lidocaine. The label shows the product name, active ingredient strength, and indicates it is a topical anesthetic cream. Additional text mentions it is clinically tested with rapid onset and uses a Derma-Release Delivery System. The net weight is 2 oz (56 g). Labeler is BioChemics, Inc.*

* 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.