Tempo Sting Relief Pad
Product Images NDC 71756-8090

3 FDA label images from Tempo Medical Products · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Tempo Sting Relief Pad (NDC 71756-8090). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Tempo Medical Products, 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

71756-8010-1 Pouch (8010 Pouch)

71756-8010-1 Pouch (8010 Pouch)
Tempo BZK Towelette labeling shows front and back of a single-use alcohol prep pad pouch. The front panel includes the product name, manufacturer Tempo Medical Products, NDC, manufacturing number, and indications of 70% isopropyl alcohol saturation. The back panel provides drug facts with active ingredient isopropyl alcohol 70% v/v, usage instructions, warnings, directions, and storage information.*
FDA Label Image

71756-8050-1 Pouch (8050 Pouch)

71756-8050-1 Pouch (8050 Pouch)
Tempo BZK Towelette packaging label from Tempo Medical Products, showing a single pouch design. The label includes the product name, manufacturing number 8050, and states it contains 0.13% Benzalkonium Chloride as the active ingredient. It specifies one towelette per pouch, indicates 'For External Use Only', and includes the manufacturer's contact information and address in Phoenix, AZ. Also visible is a Drug Facts panel listing active and inactive ingredients, usage instructions, warnings, and storage information.*
FDA Label Image

71756-8090-1 Pouch (8090 Pouch)

71756-8090-1 Pouch (8090 Pouch)
Tempo BZK Towelette packaging label from Tempo Medical Products in Reflex Blue and gray colors. The label shows the product name "STING RELIEF PAD" with NDC 71756-8090-1 and indicates the pouch contains one pad. Active ingredients listed are 6% Benzocaine and 70% Isopropyl Alcohol. Additional details include sterilization status, manufacturer contact, and storage temperature range. The label includes lot, expiration, and lot information.*

* 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.