Extra Strength Numbify Anorectal
Product Images NDC 69804-081

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Extra Strength Numbify Anorectal (NDC 69804-081). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ridge Properties, 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

Active Ingredients (Active Ingredients)

Label panel showing the active ingredient of Extra Strength Numbify Anorectal as Lidocaine HCl at 5% concentration. The text is white on a black background, clearly highlighting the active ingredient and its strength.*

FDA Label Image

Inactive Ingredients (Dosage And Adminstration)

A directions panel for Extra Strength Numbify Anorectal instructing users to test skin for sensitivity before use, apply thick layers every 3 minutes until pain relief is achieved, discontinue if sensitivity occurs, and not to use near eyes or on the face.*

FDA Label Image

Indications And Usage (Indications And Usage)

A section of drug facts text panel showing the heading 'Uses:' followed by the statement 'For Temporary Pain Relief.' This indicates the intended temporary pain-relieving use of the product.*

FDA Label Image

Principal Display Panel (Principal Display Panel)

Drug Facts panel for Extra Strength Numbify Anorectal, a topical anesthetic gel. The text includes warnings, uses, directions, and inactive ingredients such as water, kava kava, alcohol, acrylates C10-30 alkyl acrylate crosspolymer, and benzyl alcohol. It details professional use, cautions against use on broken skin or near eyes, and instructions to discontinue use if sensitivity occurs. The labeler Ridge Properties is mentioned along with contact information.*

FDA Label Image

Purpose (Purpose)

A drug facts panel segment showing the purpose of the product as a topical anesthetic. The text includes the heading "Purpose:" followed by "Topical Anesthetic" on a black background with white letters.*

FDA Label Image

Warnings (Warnings Section)

Warning label panel from Extra Strength Numbify Anorectal advising to keep out of reach of children, for external use only, not for use around eyes, and to seek medical help if ingested. It instructs users to stop use and consult a doctor if skin irritation occurs or symptoms worsen or persist beyond seven days.*

FDA Label Image

Inactive Ingredient Section (Inactive Ingredient Section)

Inactive ingredients panel for Extra Strength Numbify Anorectal lists Alcohol, Water, Kava Kava, Acrylates C10-30 Alkyl Acrylate Crosspolymer, and Benzyl Alcohol as inactive components.*

FDA Label Image

Keep Out Of Reach Of Children (Keep Out Of Reach Of Children)

A warning label panel stating: Keep out of reach of children. For external use only. Not for use around the eyes.*

* 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.