Standardized Mite Dermatophagoides Pteronyssinus
Product Images NDC 36987-1845

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Standardized Mite Dermatophagoides Pteronyssinus (NDC 36987-1845). 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 Std Mite Scratch (Nelco 5 mL Std Mite Scratch)

Label for Standardized Mite Dermatophagoides pteronyssinus allergenic extract from Nelco Laboratories, Inc. The vial is a 5 mL multiple dose container with a potency of 10,000 AU/mL. The label includes storage instructions to keep the product at 2° to 8°C and lists preservatives phenol 0.4% and glycerin 50% (w/v). It also notes U.S. Government License No. 459 and cautions against dispensing without prescription.*

FDA Label Image

Std Mite Intradermal (Nelco Std Mite Intradermal)

Label for Standardized Mite Dermatophagoides pteronyssinus allergenic extract by Nelco Laboratories, Inc. It indicates intradermal testing use, with placeholders for concentration, glycerin percentage, allergenic units per mL, lot number, and expiration date. The label includes storage instructions and cautions against dispensing without prescription.*

FDA Label Image

Std Mite Therapeutic (Nelco Std Mite Therapeutic)

Label for Standardized Mite Dermatophagoides pteronyssinus allergenic extract, manufactured by Nelco Laboratories, Inc. The label includes concentration of 50% glycerin (v/v), and space for lot number and expiration date. Directions mention storage at 5°C ± 3°C and typical dose volume of 0.05 mL.*

* 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.