California Mugwort
Product Images NDC 36987-3282

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for California Mugwort (NDC 36987-3282). 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 of an allergenic extract product by Nelco Laboratories, Inc. The label states it is for intradermal testing and is a 5 mL sterile multiple dose vial. The label includes regulatory caution about federal law and storage instructions for the product.*

FDA Label Image

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

Label for California Mugwort allergenic extract 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 notes compliance with U.S. standards for phenol and glycerin concentration and contains cautionary information about federal law restrictions on dispensing.*

FDA Label Image

Stock Concentrate Large Label (Nelco Stock Concentrate Large Label)

Label from a multiple dose vial of Allergenic Extract by Nelco Labs Inc. designed for intradermal testing. The label includes spaces for lot number and expiration date, and states storage instructions and caution regarding dispensing without prescription. The label specifies U.S. government license number 459 and Nelco Labs' address in Deer Park, NY.*

FDA Label Image

Stock Concentrate Small Label (Nelco Stock Concentrate Small Label)

Label for California Mugwort allergenic extract by Nelco Laboratories, Inc. The label is blue and white, marked as a sterile multiple dose vial with U.S. government license number 459. It includes cautions about federal law, prescription requirements, and dilution instructions, and shows the labeler 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.