Apricot
Product Images NDC 36987-1286

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Apricot (NDC 36987-1286). 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 Apricot allergenic extract by Nelco Laboratories, Inc. The label indicates it is for intradermal testing and identifies the product as a sterile multiple dose vial of 5 mL. It includes warnings about federal law and storage instructions.*

FDA Label Image

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

Apricot AllergeniC Extract for Scratch Testing in a 5 mL multiple dose vial by Nelco Laboratories, Inc. The label includes storage instructions at 2-8°C and cautions regarding federal legal restrictions and usage details, with the labeler's address in Deer Park, NY.*

FDA Label Image

Stock Large Label (Nelco Stock Concentrate Large Label)

Label for Apricot allergenic extract by Nelco Laboratories, Inc., indicating sterile multiple dose vial for intradermal testing. The label includes space for lot number and expiration date with usage and storage instructions, and bears the address of Nelco Labs in Deer Park, NY.*

FDA Label Image

Stock Small Label (Nelco Stock Concentrate Small Label)

Label for Apricot Allergenic Extract by Nelco Laboratories, Inc., showing a sterile multiple dose vial indication and U.S. government license number. Includes caution, warning, and storage instructions, as well as company 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.