Para Grass Pollen
Product Images NDC 36987-2347

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Para Grass Pollen (NDC 36987-2347). 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 Para Grass Pollen allergenic extract by Nelco Laboratories, Inc. The label shows it is for intradermal testing and a sterile multiple dose vial. It includes caution about federal law prohibiting dispensing without prescription. Manufacturer address and storage instructions are also present.*

FDA Label Image

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

Packaging label for Para Grass Pollen Allergenic Extract by Nelco Laboratories, Inc. The label specifies it is for scratch testing and is contained in a 5 mL multiple dose vial. Storage instructions include keeping the product at 2-8°C and it contains 0.4% phenol and 50% glycerin as preservatives.*

FDA Label Image

Stock Concentrate Large Label (Nelco Stock Concentrate Large Label)

Label for Para Grass Pollen allergenic extract sterile multiple dose vial by Nelco Laboratories, Inc. The label includes instructions for intradermal testing, lot number, and expiration date fields, and states the product should be stored at 4°C to 3°C. It also notes federal law prohibits dispensing without a prescription.*

FDA Label Image

Stock Concentrate Small Label (Nelco Stock Concentrate Small Label)

Label for Para Grass Pollen allergenic extract by Nelco Laboratories, Inc., showing a blue border and text. It includes usage warnings, dosage and storage instructions, and the company's address in Deer Park, NY. The label mentions it is a sterile multiple dose vial under U.S. government license number 459.*

* 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.