Zpol Ultra Cream
Product Images NDC 55715-008

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Zpol Ultra (NDC 55715-008). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Laboratorios Zepol S.a., 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

Zepol Ultra 119g (Etiqueta Zepol Ultra 119g Ing 001)

Zpol ULTRA Topical Analgesic Cream label in a blue background, showing active ingredients Menthol 2.84% and Methyl Salicylate 18.24%, with directions for use and warnings. The label states it is for external use, made by Laboratorios Zepol S.A., and provides contact details including phone and website. The net weight is 4.02 oz.*

FDA Label Image

Zepol Ultra 29g (Etiqueta Zepol Ultra 29g Ing 001)

Label for Zpol ULTRA topical analgesic cream, 1.02 oz, manufactured by Laboratorios Zepol S.A. The active ingredients are Menthol and Methyl Salicylate. The label includes Drug Facts with active ingredients, uses, warnings, directions, and other information. It provides manufacturer contact details and a barcode with the NDC 55715-008.*

FDA Label Image

Zepol Ultra 59g (Etiqueta Zepol Ultra 59g Ing 001)

Label for Zpol ULTRA topical analgesic cream by Laboratorios Zepol S.A., containing Menthol and Methyl Salicylate. The label indicates a 2.08 oz tube, with active ingredient strengths of 2.84 to 18.24 g/100g. It includes Drug Facts, usage instructions, warnings, manufacturer information, customer service contacts, and a barcode.*

* 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.