Extra Strength Numbify Anorectal
Product Images NDC 69804-079

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 69804-079). 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

Principal Display Panel (4 Oz Spray)

Extra Strength Numbify Anorectal nasal spray label showing 5% lidocaine HCL active ingredient with a net content of 4 ounces. The label includes warnings, directions, and ingredients such as water, kava kava, alcohols C10-30 alkyl acrylate crosspolymer, and benzyl alcohol. The labeler is ridge properties and the product NDC is 69804-079-04.*

FDA Label Image

Dosage And Administration (Dosage And Administration)

A directions panel instructing to test skin for sensitivity prior to use, apply thick layers every 3-5 minutes until desired pain relief is reached, discontinue if sensitivity occurs, and warning that it is not for use on or near the eyes.*

FDA Label Image

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

A warning panel for Extra Strength Numbify Anorectal states to keep out of reach of children, for external use only, and not for use around the eyes. It advises seeking medical help or poison control if ingested, and stopping use and consulting a doctor if skin irritation occurs, symptoms worsen, last over 7 days, or symptoms clear then return within a few days.*

FDA Label Image

Otc Active Ingredients Section (Otc Active Ingredients Section)

A drug facts panel highlighting the active ingredient section, showing Lidocaine HCL at 5% concentration.*

FDA Label Image

Otc Purpose Section (Otc Purpose Section)

Drug Facts panel section highlighting the purpose of Extra Strength Numbify Anorectal as a topical anesthetic. The text is white on a black background and emphasizes 'Purpose' in bold followed by 'Topical anesthetic.'*

FDA Label Image

Warnings (Warnings Section)

Warning label panel for Extra Strength Numbify Anorectal from ridge properties, advising to keep out of reach of children, for external use only, not for use around eyes, and instructions to seek medical help or call poison control if ingested. It also advises stopping use and consulting a doctor if skin irritation occurs, symptoms worsen, last longer than 7 days, or return after clearing.*

FDA Label Image

Inactive Ingredient Section (Inactive Ingredient Section)

Text panel listing inactive ingredients for Extra Strength Numbify Anorectal, including Alcohol, Water, Kava Kava, Acrylates C10-30 Alkyl Acrylate Crosspolymer, and Benzyl Alcohol, on a black background with white text.*

FDA Label Image

Indications And Usage (Indications And Usage)

A drug facts panel section titled 'Uses,' stating that the product is for the 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.