T-o-s Standardized Grass Pollen Mix Solution
Product Images NDC 22840-0227

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 35 technical images submitted to the FDA as part of the official labeling for T-o-s Standardized Grass Pollen Mix (NDC 22840-0227). 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

0200 4 Bermuda 10000 Bau

0200 4 Bermuda 10000 Bau
This is a description of Sterle Multiple Dose Vsl, which is a US prescription-only medication used for allergies caused by grass pollen. The specific allergenic ingredient in this medication is Bermuda grass pollen (Cynodon dactylon), which is standardized to 10000 AU/t. The medication is recommended to be stored at a temperature of 24°C. There is mention of a code (0032284000085) and a date (23 May 2019) but it is unclear what they pertain to.*
FDA Label Image

0201 2 Kentucky Blue June 10000 Bau

0201 2 Kentucky Blue June 10000 Bau
This is a description of an allergenic extract that is a standardized grass pollen specifically Kentucky Blue/June with the scientific name Poa protensis = em GT16A06. The extract comes in 10 mL and contains S Grear.se Pcoge s. The remaining text seems to be codes that do not provide useful information.*
FDA Label Image

0202 5 Kentucky Blue June 100000 Bau

FDA Label Image

0203 2 Meadow Fescue 10000 Bau

0203 2 Meadow Fescue 10000 Bau
This is a description for an allergenic extract of standardized grass pollen from meadow fescue (Festuca elatior). The extract has 10,000 allergen units per milliliter (AU/t) and comes in a 10mL vial with the product code GT14ADS. No further information can be gathered from the text.*
FDA Label Image

0204 4 Meadow Fescue 100000 Bau

0204 4 Meadow Fescue 100000 Bau
Standardized grass pollen allergenic extract for multiple doses is available in the US by prescription only. It contains meadow fescue at a concentration of 100,000 sAU/mL, obtained from Festuca elatior. The product is labeled with a product code and batch number, as well as storage instructions to be kept at 24°C. The manufacturer is GRSER, located in Lok, HC286AS U, ket 308.*
FDA Label Image

0205 5 Orchard 10000 Bau

FDA Label Image

0206 2 Orchard 100000 Bau

FDA Label Image

0207 4 Redtop 10000 Bau

FDA Label Image

0208 2 Redtop 100000 Bau

FDA Label Image

0209 5 Perennial Rye 10000 Bau

FDA Label Image

0210 4 Perennial Rye Grass 100000 Bau

0210 4 Perennial Rye Grass 100000 Bau
This is a description of a standardized grass pollen allergenic extract called "Sterle Multiple Dose Visl". It is only available in the US with a prescription and must be stored at a temperature of 24 degrees Celsius. The extract contains Perennial Rye grass pollen with a potency of 100,000 Allergy units. The package size is 50 tablets with the code GT24AD2. The extract contains SON G and may also contain other substances that are not listed. The expiration date is July 23, 2019.*
FDA Label Image

0211 5 Sweet Vernal 10000 Bau

FDA Label Image

0212 4 Sweet Vernal Grass 100000 Bau

FDA Label Image

0213 2 Timothy 10000 Bau

FDA Label Image

0214 4 Timothy 100000 Bau

0214 4 Timothy 100000 Bau
This appears to be a label of a Sterile Multiple Dose Vial of an Allergenic Extract, in this case for Standardized Grass Pollen (Timothy 100,000 840/t) including Phieum pratense. The vial is intended for US RxOnly and must be stored at 2.4°C. Other information such as the manufacturer's information, lot and batch numbers, and date of production are also present.*
FDA Label Image

0215 5 Timothy Orchard Grass 100000 Bau

FDA Label Image

0216 2 Kot Grass 10000 Bau

0216 2 Kot Grass 10000 Bau
This is a description of an allergenic extract standardized grass pollen mix that comes in a multiple-dose vial, which is only available with a prescription in the United States. It is recommended to store at 24°C. The extract contains equal parts of three standardized grass pollens, including Kotgrass. The potency of the extract is 10,000 BAU/L. The package insert should be consulted for information on contraindications and suggested usage directions. The expiration date for the product is May 23, 2007.*
FDA Label Image

0217 4 Kot Grass 100000 Bau

FDA Label Image

0218 5 Kort Grass 10000 Bau

0218 5 Kort Grass 10000 Bau
The text appears to be a product label for an allergenic extract containing standardized grass pollen mix with a potency of 10,000 BAU/mL. It also includes information regarding the product's preservation and content warnings.*
FDA Label Image

0219 2 Kort Grass 100000 Bau

0219 2 Kort Grass 100000 Bau
The text describes a product, the standardized grass pollen mix, specifically for Kortgrass. It contains equal parts of four standardized grass pollens. The cumulative potency is 911100000 BAU/mt. It has a 0.4% preservative and 0% glycerin. The package provides instructions for use and dosage. The rest of the text appears to be unreadable or not relevant.*
FDA Label Image

0220 4 Kort Sv Grass 10000 Bau

0220 4 Kort Sv Grass 10000 Bau
This is a description of an allergenic extract. The standardized grass pollen mix containing Kortand sweet vernal grass in equal parts is stored at 24°C in a store that is only accessible to those with a prescription. The extract also contains sandradized grass pollens as well as GTrESAda S0t and has a concentration of 1000 AUk. It is recommended to check the package insert for contents and dosage information. The manufacturer appears to be R Leborerto and their address is listed as Lanch N 248 U1, Lcomaa 108. The date on the document is May 23, 2019.*
FDA Label Image

0221 2 Kort Sv Grass 100000 Bau

0221 2 Kort Sv Grass 100000 Bau
Standardized Grass Pollen Mix Immunotherapy extract containing equal parts of K-O-A-T and sweet vernal grass with cumulative potency up to 100,000 8AU/m. It contains 0% Phenol as a preservative and 5054/v Gheenin. Refer to package insert for usage instructions and dosage directions. Lot number 10 Sample was produced on May 23rd, 2019.*
FDA Label Image

0222 5 7 Grass 10000 Bau

0222 5 7 Grass 10000 Bau
This is a description of an allergenic extract standardized grass pollen mix. It contains seven standardized grass pollens in equal parts and has a potency of 100,000 BAU/mi. The extract also contains Phenol and 50% v Glycenn. The package insert contains comments, dose, and directions for use. The expiry date of the product is May 23, 2018.*
FDA Label Image

0223 4 7 Grass 100000 Bau

0223 4 7 Grass 100000 Bau
This is a product label for an allergenic extract of a standardized mix of grass pollen. The extract is intended for medical use and contains a specific amount of grass pollen measured in BAU. The label provides directions for use, but no further details are available.*
FDA Label Image

0224 5 Tos Grass 10000 Bau

FDA Label Image

0225 2 9 Southern Grass Mix Conc

FDA Label Image

0225 4 9 Southern Grass Mix Conc

FDA Label Image

0225 5 9 Southern Grass Mix Conc

FDA Label Image

0226 2 Timothy Orchard Grass 10000 Bau

0226 2 Timothy Orchard Grass 10000 Bau
This appears to be a description of an allergenic extract, specifically a standardized grass pollen mix which contains equal parts of two standardized grass pollens - Timothy-Orchard Grass. The extract is available in a multi-dose vial and has a cumulative potency of 10,000 BAU/mL. The extract may contain S04 /v Gheanin and package insert should be consulted for dosage and administration instructions. There is also a code VAR 60 (17) 33y 200 at the end of the text, which may be a reference number.*
FDA Label Image

0227 5 Tos Grass 100000 Bau

FDA Label Image

Figure 1

FDA Label Image

Figure 2

Figure 2
This appears to be a medical record or report indicating that a patient was suspected to have a systemic allergic reaction and was tested using percutaneous skin testing with varying amounts of BAU/mL extract. The record also notes that positive and negative control applications should be used during future skin tests.*
FDA Label Image

Length And Midpoint Orthogonal Width

Length And Midpoint Orthogonal Width
This is a description of wheal and flare reactions. A wheal is a smooth, slightly elevated area that can be either redder or paler than the surrounding skin, while the flare is the red outermost zone of a wheal reaction.*
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.