Extra Strength Numbify Anorectal
Product Images NDC 69804-080

8 FDA label images from Ridge Properties · Packaging, Regulatory Labels, and Product Appearance

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 69804-080). 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)

Active Ingredients (Active Ingredients)
Text panel displaying the active ingredient information for a product, stating 'Active Ingredient: Lidocaine HCL 5%'.*
FDA Label Image

Dosage And Administration (Dosage And Adminstration)

Dosage And Administration (Dosage And Adminstration)
Directions panel for Extra Strength Numbify Anorectal, instructing users to test skin for sensitivity prior to use, apply thick layers every 3 minutes until desired pain relief is reached, discontinue if sensitivity occurs, and warning not to use near eyes or on the face.*
FDA Label Image

Inactive Ingredients (Inactive Ingredient Section)

Inactive Ingredients (Inactive Ingredient Section)
A text panel listing inactive ingredients of Extra Strength Numbify Anorectal, including Alcohol, Water, Kava Kava, Acrylates C10-30 Alkyl Acrylate Crosspolymer, and Benzyl Alcohol.*
FDA Label Image

Indications And Usage (Indications And Usage)

Indications And Usage (Indications And Usage)
Drug Facts text panel titled 'Uses,' stating the product is for temporary pain relief. The panel background is black with white text.*
FDA Label Image

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

Keep Out Of Reach Of Children (Keep Out Of Reach Of Children)
A warning panel stating: Keep out of reach of children. For external use only. Not for use around the eyes. The text is white on a black background and emphasizes safety precautions for external use products.*
FDA Label Image

Purpose (Purpose)

Purpose (Purpose)
A text panel titled 'Purpose:' indicating the product's use as a 'Topical Anesthetic.' This panel is likely part of the drug facts or purpose section of the product labeling for Extra Strength Numbify Anorectal.*
FDA Label Image

Warnings (Warnings Section)

Warnings (Warnings Section)
Warning text panel from Extra Strength Numbify Anorectal product by ridge properties. It advises to keep the product out of reach of children, restricts use to external only, and cautions against use around eyes. It instructs to seek immediate medical help or poison control if ingested, and to stop use and consult a doctor if skin irritation develops, symptoms worsen, last beyond 7 days, or reoccur after clearing.*
FDA Label Image

Principal Display Panel (Principal Display Panel)

Principal Display Panel (Principal Display Panel)
Drug Facts label for Extra Strength Numbify Anorectal cream showing professional use only. Active ingredient is Lidocaine HCL 5%. Inactive ingredients include Alcohol, Water, Kava Kava, Mica Powder, Acrylates C10-30 Alkyl Acrylate Crosspolymer, and Benzyl Alcohol. Directions note to test skin sensitivity and avoid contact with eyes. Warnings emphasize external use only, not near eyes, and to keep out of reach of children. Product is a topical anesthetic intended for temporary relief of topical pain.*

* 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.