Neurospora Intermedia
Product Images NDC 36987-2013

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Neurospora Intermedia (NDC 36987-2013). 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 an allergenic extract for intradermal testing from Nelco Laboratories, Inc. The label includes a blank white space presumably for specific product or batch details. It notes a usual initial dose of 0.05 mL and storage instructions between 2-8°C. The label states it is sterile, multiple dose vial with U.S. and Canadian license information.*

FDA Label Image

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

Alternaria alternata allergenic extract label for scratch testing by Nelco Laboratories, Inc. The label specifies a 5 mL multiple dose vial and includes storage instructions at 2-8°C. It also contains a federal law caution against prescription use without a doctor's order and a note about the solution containing phenol, glycerin, and water.*

FDA Label Image

Stock Concentrate Large Label (Nelco Stock Concentrate Large Label)

Label for Alternaria alternata allergenic extract by Nelco Laboratories, Inc., intended for intradermal testing. The sterile multiple dose vial label includes spaces for lot number and expiration date, cautioning against dispensing without prescription and providing storage instructions.*

FDA Label Image

Stock Concentrate Small Label (Nelco Stock Concentrate Small Label)

Label for Alternaria alternata allergenic extract from Nelco Laboratories, Inc. The blue label includes instructions noting it is a sterile multiple dose vial, U.S. government license number, caution that federal law prohibits dispensing without prescription, and warnings to use only as directed with appropriate dilution. The label includes the manufacturer's address in Deer Park, NY.*

* 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.