Figure 1 (Figure 1)
Cromolyn Sodium
Product Images NDC 72162-1934
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Cromolyn Sodium (NDC 72162-1934). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Bryant Ranch Prepack, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Figure 2 (Figure 2)
Figure 3 (Figure 3)
Figure 4 (Figure 4)
Label (Lbl721621934)
This is a description for a medication called Cromolyn Sodium Oral Solution (Concentrate). Each 5 mL ampule contains 100 mg of Cromolyn Sodium, which is to be used orally and not for inhalation or injection. The medication must be diluted before use. It should be stored at a temperature between 20°C to 25°C (68°F to 77°F), protected from light. Do not use if the solution contains a precipitate or if it becomes discolored. It should be kept out of the reach of children and stored in its foil pouch until ready to use. The National Drug Code (NDC) for this medication is 72162-1934-2. The ampules are manufactured by Bryant Ranch Prepack, Inc. and relabeled by Woodward Pharma Services.*
Recycle Figure (Recycle Figure)
Cromolyn Structure (Structure)
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
