Superior Pain And Itch Relief
Product Images NDC 69804-071

8 FDA label images from Ridge Properties Llc · 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 Superior Pain And Itch Relief (NDC 69804-071). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ridge Properties Llc, 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

Dosage And Administration (Dosage And Administration)

Dosage And Administration (Dosage And Administration)
Directions text panel for Superior pain and itch relief by ridge properties llc. The panel instructs to test skin for sensitivity before use, discontinue if sensitivity occurs, apply thick even layers every 3-5 minutes until desired pain relief, and avoid use near the eyes.*
FDA Label Image

Inactive Ingredients (Inactive Ingredients Section)

Inactive Ingredients (Inactive Ingredients Section)
Inactive ingredients panel listing Propylene Glycol, Water, Kava Kava, Copaiba Balsam, Acrylates C10-30 Alkyl Acrylate Crosspolymer, and Benzyl Alcohol. This information is associated with Superior pain and itch relief by ridge properties llc.*
FDA Label Image

Indications And Usage (Indications And Usage)

Indications And Usage (Indications And Usage)
A text panel titled 'Uses' stating that the product provides temporary relief of pain and itching. The phrase 'Uses - For temporary relief of pain and itching' is displayed in green text on a black background.*
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 drug warning text panel with the message advising to keep the product out of reach of children, for external use only, and not for use around the eyes. It instructs to seek medical help or call poison control immediately if ingested.*
FDA Label Image

Active Ingredient (Otc Active Ingredient)

Active Ingredient (Otc   Active Ingredient)
A drug facts panel showing the active ingredient as Lidocaine HCL at a concentration of 4%. The text is displayed in green font on a black background, emphasizing the active ingredient information.*
FDA Label Image

Purpose (Purpose)

Purpose (Purpose)
A text panel displaying the purpose section with the purpose stated as "Topical Anesthetic" in green font, highlighting the intended use of the product for topical anesthesia.*
FDA Label Image

Warnings Section (Warnings Section)

Warnings Section (Warnings Section)
A warning text panel for Superior pain and itch relief by ridge properties llc. It advises keeping the product out of reach of children, external use only, avoiding use around the eyes, and seeking immediate medical help or poison control if ingested. It also instructs to stop use and consult a doctor if skin irritation or worsening occurs, symptoms last more than 7 days, or symptoms clear up and then return.*
FDA Label Image

Principal Display Panel (Principal Display Panel)

Principal Display Panel (Principal Display Panel)
Drug Facts panel for Superior pain and itch relief by ridge properties llc. It includes directions for use as a 4 ounce spray for topical anesthetic lidocaine HCL. The label provides warnings, usage instructions, active and inactive ingredients, and contact information. Key warnings include KEEP OUT OF REACH OF CHILDREN and avoiding use near eyes. Ingredients listed include Lidocaine HCL as active and propylene glycol, water, kava kava, copaiba balsam, acrylates, and benzyl alcohol as inactive.*

* 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.