Aureobasidium Pullulans Solution
Product Images NDC 22840-5607

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Aureobasidium Pullulans (NDC 22840-5607). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Greer 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

1600 2 Alternaria Alternata 20000 Pnu

This is a description of a sterile multiple dose vial containing an allergenic extract of Alternaria alternata, with a volume of 10mL and a potency of 20,000 PNU/mL. The vial should be stored at 246 and has a preservative of 0.4% Phenol. There is no U, but the standard of potency can be found in the package insert. The DIN is 02372428, the GTIN is 00322840160028, and the LOT number is not readable. The expiration date is January 1, 2025. This vial was manufactured by REER Laboratories Inc. located in Lenolr, NC with U.S. License 308.*

FDA Label Image

1628 1 Aspergillus Niger 1000 Wv

This is a description for an Allergenic Extract of Aspergillus niger, which comes in a sterile multiple dose vial for U.S. use only. It should be stored between 2-8°C and has a 0.4% Phenol preservative. There is no U.S. standard of potency, and the package insert should be consulted for details on content, dosage, and usage directions. The lot number is listed as SAMPLE, the expiration date is Jan 1, 2025, and it has a National Drug Code of 22840-1628-1. The product is manufactured by Greer Laboratories Inc. in Lenoir, NC with a U.S. License of 308.*

FDA Label Image

5610 4 Candida Albicans 20 Wv

This is a description of an allergenic extract of Candida albicans in a sterile multiple dose vial. The vial is intended for U.S prescription use and must be stored at a temperature of 2-8°C. It contains 50mL of 1:20 WV solution with 0.2% phenol as a preservative and 50% v/v glycerin. There is no U.S. standard of potency provided, and more information can be found in the package insert regarding the contents, dosage, and directions for use. The product has a GTIN of 00322840561047, an S/N of 00000000000, and a LOT of SAMPLE. It is set to expire on January 1st, 2025. This is produced by GREER Laboratories, Inc., and is licensed for use in the United States.*

FDA Label Image

9641 5 Fusarium Mix 40 Wv

This is a description of an allergenic extract called Fusarium Mix, designed for skin testing purposes only and available only by prescription in the US. The extract contains a mix of Gibberella fujikuroi and Fusarium solani, and comes in a vial with the product code GMO9A01. It is preserved with 0.2% Phenol and contains 50% v/v Glycerin. There is no US standard of potency for this product, and customers are directed to reference the package insert for contents, dosage, and directions for use. The expiry date for this batch is January 1, 2025. The producer is Greer Laboratories, Inc., located in Lenoir, NC and licensed under number 308.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.