Balsam Poplar
Product Images NDC 36987-3120

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Balsam Poplar (NDC 36987-3120). 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 Intradermal (Nelco 5 mL Stock Concentrate Intradermal)

Label for Red Alder allergenic extract by Nelco Laboratories, Inc., intended for intradermal testing. The label states it is a sterile multiple dose vial with instructions on dosage and storage, including a usual initial dose of 0.05 mL and storage at 2° to 8°C. The label includes caution about federal law prohibiting dispensing without prescription.*

FDA Label Image

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

Label of Red Alder allergenic extract by Nelco Laboratories, Inc. The label specifies it is for scratch testing. It includes storage instructions at 2-8°C and mentions a phenol concentration of 0.4% and glycerin at 50%. The label also contains a caution about federal law prohibiting dispensing without prescription and usage instructions for individual doses as drops in a closed circuit.*

FDA Label Image

Stock Large Label (Nelco Stock Concentrate Large Label)

Label for Red Alder allergenic extract by Nelco Laboratories, Inc. The sterile multiple dose vial is for intradermal testing. The label includes spaces for lot number and expiration date, with usage and storage instructions, and the manufacturer address in Deer Park, NY.*

FDA Label Image

Stock Small Label (Nelco Stock Concentrate Small Label)

Label from a sterile multiple dose vial of Red Alder allergenic extract by Nelco Laboratories, Inc. It includes cautionary and storage instructions, the company's address in Deer Park, NY, and specifies U.S. Government License No. 459. The label has a blue border with white text and a blank white central area likely for additional vial-specific details.*

* 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.