Sunflower Solution
Product Images NDC 22840-1503

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Sunflower (NDC 22840-1503). 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

1502 1 Dandelion 1000 Wv

1502 1 Dandelion 1000 Wv
This is an allergenic extract medication designed for U.S. consumers containing Dandelion Pollen (Taraxacum officinale). It is a sterile multi-dose vial which should be stored in temperatures between 2°C to 8°C. The item number is 159A10, with a strength of SmL 1:1,000 W/V and preservative content of 0.4% Phenol, identified with a DIN 02372444. No US standard of potency is available, with the package insert containing information on contents, dosage, and directions for use. The vial has a GTIN (01) identification number of 0322840150210, a serial number (21) of 000000000000, and a LOT number (10) of SAMPLE. Its expiration date is on Jan 01, 2025, and it has an NDC 22840-1502- identification number. Produced by GREER Laboratories, Inc. with a U.S. License 308, based in Lenoir, NC 28645.*
FDA Label Image

1504 2 Sunflower 40000 Pnu

1504 2 Sunflower 40000 Pnu
This is a description of a sterile multiple dose vial of allergenic extract containing sunflower pollen with a potency of 40,000 PNU/mL and 0.4% Phenol. The product has no U.S Standard of potency, and the DIN number is 02372444. It is important to read the package insert for directions on use, contents, and dose. The GTIN number is 00322840150425, S/N number is 000000000000, lot number is SAMPLE 8, and the expiration date is 01Jan 2025. The manufacturer of this product is GREER Laboratories, Inc., and its U.S. license number is 308.*
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5500 5 Daisy 20 Wv

5500 5 Daisy 20 Wv
This is a skin test allergenic extract vial for Daisy Pollen. It contains Leucanthemum vulgare and has a strength of 1:220 W/V. It has a preservative 0.2% Phenol and 50% v/v Glycerin. The package insert provides details on the contents, dose, and directions for use. The vial has a 3% GTIN and an expiration date of January 1, 2025. It is produced by GREER Laboratories and has a lot number of SAMPLE. Store this product at 2.8°C until use.*
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5502 4 Sunflower 20 Wv

5502 4 Sunflower 20 Wv
This is a description of a product called "ALLERGENIC EXTRACT" which is a sterile multiple dose vial used by prescription in the United States. It contains SUNFLOWER POLLEN 3 (Helianthus annuus 2) and has a size of 50 mL with a 0.2% Phenol preservative. It also has 50% v/v Glycerin and no U.S. Standard of Potency. The package insert contains information on the contents, dose, and directions for use. It has a GTIN of (01) 00322840550249 and a S/N of (21) 000000000000. Its LOT is SAMPLE 8, and the EXP date is 01 Jan 2025. The manufacturer is GREER Laboratories, Inc., located in Lenolr, NC28645, where it holds a U.S. License.*
FDA Label Image

Figure 1

FDA Label Image

Figure 2

FDA Label Image

Length And Midpoint Orthogonal Width

Length And Midpoint Orthogonal Width
This text provides a basic definition and explanation of the wheal and flare reaction that can occur on the skin in response to an allergic or immune system reaction. The wheal is described as a smooth, slightly elevated area that appears different from the surrounding skin, while the flare is the red outermost zone surrounding the wheal.*
FDA Label Image

Measure The Flare

FDA Label Image

Measuring The Wheal

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