Standardized Perennial Rye Grass Injection
Product Images NDC 49643-379

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Standardized Perennial Rye Grass (NDC 49643-379). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Allermed 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

0309 50 Std Redtop Grass 50ml

0309 50 Std Redtop Grass 50ml
Label for Standardized Sweet Vernal Grass injection, containing allergenic extract with 100,000 BAU/mL concentration. The product is supplied in a 50 mL container and labeled by Allermed Laboratories, Inc. The label includes storage instructions, the route of administration as cutaneous, intradermal, and subcutaneous, and contact information for AllerMed in San Diego, CA.*
FDA Label Image

0318 10 Std Sweet Vernal Grass 10ml

0318 10 Std Sweet Vernal Grass 10ml
Label for Standardized Sweet Vernal Grass Allergenic Extract injection by Allermed Laboratories, Inc. Contains Anthoxanthum odoratum at a strength of 100,000 BAU/mL in a 10 mL vial. The label shows preservative content and directions for use, the labeler name, address in San Diego, CA, contact number, and license information, along with expiration and lot details.*
FDA Label Image

0342 10 Std Bermuda Grass 10ml

0342 10 Std Bermuda Grass 10ml
Label for Standardized Sweet Vernal Grass allergenic extract injection, 10,000 BAU/mL strength, from Allermed Laboratories, Inc. The vial contains 10 mL. The label includes storage instructions (4-28°C), prescription-only designation, and contact information for AllerMed in San Diego, CA.*
FDA Label Image

0343 10 Std Orchard Grass 10ml

0343 10 Std Orchard Grass 10ml
Label for Standardized Sweet Vernal Grass allergenic extract injection, strength 100,000 BAU/mL, containing 10 mL. The label includes botanical names (0343 Std. Orchard Grass, Dactylis glomerata), manufacturer Allermed Laboratories, Inc. San Diego, CA, with contact information and storage instructions. The product is for prescription use only.*
FDA Label Image

0350 50 Std Meadow Fescue 50ml

0350 50 Std Meadow Fescue 50ml
Label for Standardized Sweet Vernal Grass allergenic extract injection, containing 100,000 BAU/mL. The label mentions 50 mL volume and identifies the product as Festuca elatior, a type of meadow fescue grass. The labeler is AllerMed Laboratories, Inc., located in San Diego, CA, with contact number 800-221-2748.*
FDA Label Image

0379 05 Std Perennial Rye Grass 5ml

0379 05 Std Perennial Rye Grass 5ml
Label of Standardized Sweet Vernal Grass allergenic extract injection, 100,000 BAU/mL strength, in a 5 mL vial. The label indicates it is a perennial rye grass extract by AllerMed Laboratories, Inc., San Diego, CA, with storage instructions and contact information included.*
FDA Label Image

0386 05 Std Timothy Grass 5ml

0386 05 Std Timothy Grass 5ml
Standardized Sweet Vernal Grass Allergenic Extract injection vial label showing 5 mL volume with 100,000 BAU/mL strength. The label includes the product type as allergenic extract and Phleum pratense species. Manufacturer is Allermed Laboratories, Inc., San Diego, CA.*
FDA Label Image

0393 05 Std Kentucky Blue Grass 5ml

0393 05 Std Kentucky Blue Grass 5ml
Packaging label for Standardized Sweet Vernal Grass allergenic extract injection, containing 100,000 BAU/mL in a 5 mL vial. Labeled for human prescription use by Allermed Laboratories, Inc., San Diego, CA. The label includes instructions to store at 2-25°C and restrict use to prescription only, with contact information and a QR code.*

* 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.