English Plantain
Product Images NDC 36987-3325

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for English Plantain (NDC 36987-3325). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nelco Laboratories, 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

5 mL Stock Concentrate Intradermal (Nelco 5 mL Stock Concentrate Intradermal)

Label for Allscale allergenic extract for intradermal testing by Nelco Laboratories, Inc. The label states it is a sterile multiple dose vial of 5 mL, with caution regarding federal law on dispensing without prescription. Instructions note usual initial dose and storage conditions.*

FDA Label Image

5 mL Stock Concentrate Scratch (Nelco 5 mL Stock Concentrate Scratch)

Allscale allergenic extract vial label from Nelco Laboratories, Inc. The label indicates the product is for scratch testing, provided in a 5 mL multiple dose vial. Storage instructions note to keep at 2-8°C. The label includes cautionary text about federal law and usual individual dosage, and the formulation contains phenol 0.4% and glycerine 50%. The label displays the manufacturer's address in Deer Park, NY.*

FDA Label Image

Stock Concentrate Large Label (Nelco Stock Concentrate Large Label)

Label of Allscale allergenic extract by Nelco Laboratories, Inc. The label states it is a sterile multiple dose vial approved by the U.S. government for intradermal testing, including fields for lot number and expiration date. It includes storage instructions and cautions about federal dispensing restrictions.*

FDA Label Image

Stock Concentrate Small Label (Nelco Stock Concentrate Small Label)

Label for Allscale, an allergenic extract product by Nelco Laboratories, Inc. The label includes a blank white space for additional information. It notes that the product is a sterile multiple dose vial under U.S. Government license No. 459. The label includes cautions about federal law prohibitions on dispensing without prescription, the need to dilute before use, and storage instructions at 2 to 8 degrees Celsius. Dosage and route details are on the product standard insert.*

* 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.