Minnerva Ii Gel
Product Images NDC 82718-2210

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Minnerva Ii (NDC 82718-2210). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Softap 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

Front Of Tube (Minnervalabel 1)

FDA Label Image

Frontlabel (Minnervalabel 2)

Frontlabel (Minnervalabel 2)
This is a description of a topical anesthetic called "Lidocaine USP- 4%" that contains ephedrine HCI-.04%, a vasoconstrictor. It is used for temporarily relieving pain associated with cuts, scrapes, or abrasions in adults over 18. The solution should not be used with occlusion, on large areas or in large quantities, and by individuals with a known allergy or sensitivity to any ingredients, pregnant or breastfeeding women, and those with a history of liver disease or impairment. If the seal of the product is broken before the first use, it should not be used.*
FDA Label Image

Insidelabel1 (Minnervalabel 3)

Insidelabel1 (Minnervalabel 3)
This is a Drug Facts label which provides information and warnings for a product produced by SofT#. It advises to avoid contact with eyes and mouth, and what to do if accidental contact occurs. The product may cause temporary rash, redness, swelling, or itching, and one may not feel pain, so sources of heat or injury should be avoided. It also warns to seek medical attention if any unusual effects occur, such as dizziness or difficulty breathing. The label includes the manufacturer's name and address.*
FDA Label Image

Labelpage3 (Minnervalabel 4)

* 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.