Letybo Injection, Powder, Lyophilized, For Solution
Product Images NDC 81165-050

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Letybo (NDC 81165-050). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hugel, Inc., 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

Carton 100 Units (Carton 100u)

LETYBO 100 units/vial injection powder label for intramuscular use containing letibotulinumtoxinA-wlbg by Hugel, Inc. The lyophilized vial label includes dosage strength, administration route, warnings, manufacturer and distributor information, barcode, and instructions for use. The label layout shows dimensions and detailed text placement on a multi-panel design.*

FDA Label Image

Carton 50 Units (Carton 50u)

Packaging label for LETYBO 50 units/vial injection, lyophilized powder for intramuscular use, containing letibotulinumtoxinA-wlbg. The label features the brand and generic names, dosage strength, usage route, and the Hugel, Inc. logo as the manufacturer. It includes dosage warnings, storage instructions, a barcode, and placeholders for lot number, expiration date, serial number, and GTIN.*

FDA Label Image

Figure 1: Letybo Sites (x) For Intramuscular Injection (Glabellar Line Injection Guide 20201208)

An anatomical diagram showing the upper face including both eyes and eyebrows. It features vertical dashed lines and "X" marks demonstrating precise anatomical points above and between the eyebrows. A double-headed arrow indicates a 1 cm vertical measurement above the left eyebrow. This illustration appears to depict specific facial landmarks likely for injection or treatment guidance.*

* 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.