Nigrospora Sphaerica
Product Images NDC 36987-2027

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nigrospora Sphaerica (NDC 36987-2027). 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 Nigrospora sphaerica allergenic extract by Nelco Laboratories, Inc. The label is predominantly blue and white, marked for intradermal testing. It includes caution about federal law prohibiting dispensing without prescription and instructions for use, specifying a 5 mL sterile multiple dose vial.*

FDA Label Image

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

Label for Nigrospora sphaerica allergenic extract by Nelco Laboratories, Inc. The label indicates it is a 5 mL multiple dose vial for scratch testing. Storage instructions specify 2 to 8°C, and it contains 0.4% phenol and 50% glycerin as a preservative. Manufacturer address is 154 Brook Ave, Deer Park, NY.*

FDA Label Image

Stock Concentrate Large Label (Nelco Stock Concentrate Large Label)

Label for Nigrospora sphaerica allergenic extract by Nelco Laboratories, Inc. It is a sterile multiple dose vial labeled for intradermal testing. The label includes fields for lot number and expiration date, and mentions storage instructions and federal law prohibiting dispensing without prescription.*

FDA Label Image

Stock Concentrate Small Label (Nelco Stock Concentrate Small Label)

Label for Nigrospora sphaerica allergenic extract from Nelco Laboratories, Inc. The label is blue with white text and includes warnings about federal law, prescription requirements, dilution instructions, and storage temperature. The label also notes the vial type and U.S. government license number.*

* 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.