Extra Strength Numbify Anorectal
Product Images NDC 69804-078

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 69804-078). 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 section showing the active ingredient of Extra Strength Numbify Anorectal as Lidocaine HCL at a concentration of 5%. The label features white text on a black background highlighting the active ingredient information.*

FDA Label Image

Dosage And Administration (Dosage And Adminstration)

Directions for Extra Strength Numbify Anorectal include testing skin sensitivity before use and applying thick layers every 3 minutes until desired pain relief is achieved. Users are advised to discontinue use if sensitivity occurs and to avoid application near the eyes or on the face.*

FDA Label Image

Inactive Ingredients (Inactive Ingredients Section)

Text panel listing inactive ingredients of Extra Strength Numbify Anorectal. The ingredients include alcohol, water, kava kava, mica powder, acrylates C10-30 alkyl acrylate crosspolymer, and benzyl alcohol.*

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Indications And Usage (Indications And Usage)

Text panel displaying a partial section titled 'Uses' indicating the product is for temporary pain relief. The text is white on a black background with part of the usage information visible.*

FDA Label Image

Principal Display Panel (Principal Display Panel)

Drug Facts label for Extra Strength Numbify Anorectal 4 Ounce Cream by ridge properties. It lists Lidocaine HCL 5% as the active ingredient and includes inactive ingredients such as alcohol, water, kava kava, mica powder, acrylates, and benzyl alcohol. The label provides directions for use, warnings, and other product information, including its professional anesthetic purpose and use for temporary topical pain relief.*

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Purpose (Purpose)

Text panel titled 'Purpose:' with the stated purpose as 'Topical Anesthetic.' This indicates the section of the label describes the intended action or use of the product.*

FDA Label Image

Warnings Section (Warnings Section)

Warning panel of Extra Strength Numbify Anorectal emphasizing to keep out of reach of children, use externally only, avoid eye contact, and seek immediate medical help if ingested. It advises to stop use and consult a doctor if skin irritation occurs, condition worsens, symptoms persist beyond 7 days, or symptoms clear and then return shortly after.*

FDA Label Image

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

A warning text panel stating: "Warning: Keep out of reach of children. For external use only. Not for use around the eyes." This panel likely comes from the packaging or labeling of Extra Strength Numbify Anorectal.*

* 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.