Alkindi Granule
Product Images NDC 71863-110

Product Visual Gallery

This gallery contains 15 technical images submitted to the FDA as part of the official labeling for Alkindi (NDC 71863-110). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eton Pharmaceuticals, 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

Structure (Hydrocortisone Structure)

Chemical structure diagram of hydrocortisone, showing its steroid backbone with multiple hydroxyl groups and ketone functional groups. The molecular structure illustrates the arrangement of carbon, hydrogen, and oxygen atoms typical for hydrocortisone.*

FDA Label Image

Image-1 (Image 1)

An instructional illustration showing a hand holding a small capsule-like granule, likely demonstrating the correct way to handle or prepare the Alkindi Sprinkle granule oral dosage form.*

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Image-2 (Image 2)

An illustration showing a hand holding a small granule, likely demonstrating how to handle or administer oral granules such as Alkindi Sprinkle (hydrocortisone) granules.*

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Image-3 (Image 3)

An instructional illustration showing a person's hands preparing to empty the contents of a granule packet by tearing it open at the top. The image is likely related to the administration of Alkindi Sprinkle oral granules.*

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Image-4 (Image 4)

An instructional illustration showing a hand sprinkling granules from a spoon onto a small curved surface, likely depicting the administration method of Alkindi Sprinkle hydrocortisone granules for oral use.*

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Image-5 (Image 5)

An instructional illustration showing a hand sprinkling granules from a small container or sachet onto a spoon. The image suggests how to administer Alkindi Sprinkle granules orally by transferring them onto a spoon for consumption.*

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Image-6 (Image 6)

An instructional illustration showing an infant receiving oral medication granules sprinkled onto the tongue using a small spoon or similar applicator. The image emphasizes oral administration suitable for children or infants.*

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Carton 0.5 mg (Alkindi Carton 0.5 mg)

Alkindi Sprinkle 0.5 mg oral granules packaging label for hydrocortisone by Eton Pharmaceuticals, Inc. The label indicates 50 capsules per package, instructs that capsules must be opened prior to administration and not swallowed whole due to choking risk. Storage instructions recommend controlled room temperature and protection from light. It also includes manufacturer information and directions to dispense an accompanying medication guide.*

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Container 0.5 mg (Alkindi Container 0.5mg)

Alkindi Sprinkle 0.5 mg oral granules packaging label showing the proprietary name, generic name hydrocortisone, strength 0.5 mg, and count of 50 capsules. The label states capsules must be opened prior to administration and warns against swallowing the capsule due to choking risk. It includes storage instructions, manufacturer Eton Pharmaceuticals, and an NDC number.*

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Carton 1 mg (Alkindi Carton 1 mg)

Alkindi Sprinkle 1 mg oral granules packaging label showing the product name, active ingredient hydrocortisone, dosage form as granules, and strength of 1 mg. The label notes that capsules must be opened prior to administration and not swallowed whole. The package contains 50 capsules. Manufacturer listed as Glatt Pharmaceutical Services GmbH & Co. KG, Germany and labeled for Eton Pharmaceuticals, Inc., Deer Park, IL. Storage instructions and barcode are also present.*

FDA Label Image

Container 1 mg (Alkindi Container 1 mg)

Label for Alkindi Sprinkle (hydrocortisone) oral granules, 1 mg strength. The label indicates 50 capsules per container and includes storage instructions to keep at controlled room temperature and protect from light. It notes that capsules must be opened before administration and warns against swallowing the capsule due to choking risk. Manufactured by Eton Pharmaceuticals, Inc.*

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Carton 2 mg (Alkindi Carton 2 mg)

Packaging label for Alkindi Sprinkle 2 mg oral granules, containing hydrocortisone. The label states capsules must be opened prior to administration and not swallowed whole due to choking risk. It includes directions to read the Medication Guide, dosage information, storage instructions, and manufacturer details for Eton Pharmaceuticals, Inc. The package contains 50 capsules.*

FDA Label Image

Container 2 mg (Alkindi Container 2mg)

Label for Alkindi Sprinkle (hydrocortisone) oral granules 2 mg, manufactured by Eton Pharmaceuticals, Inc. The label states the product contains 50 capsules, with instructions to open capsules prior to administration. Storage conditions specify controlled room temperature 20°C to 25°C with allowances between 15°C to 30°C. The label includes warnings to keep out of reach of children and discard unused portions 60 days after opening.*

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Carton 5 mg (Alkindi Carton 5 mg)

Alkindi Sprinkle 5 mg (hydrocortisone) oral granules packaging label showing 50 capsules. Label includes dosage form as oral granules, warnings not to swallow capsule due to choking risk, storage instructions, and manufacturer information for Eton Pharmaceuticals, Inc. Text advises opening capsules and sprinkling contents on tongue, spoon, or soft food before administration. Manufactured by Glatt Pharmaceutical Services, Germany.*

FDA Label Image

Container 5 mg (Alkindi Container 5mg)

Label for Alkindi Sprinkle 5 mg oral granules by Eton Pharmaceuticals, containing hydrocortisone. The label indicates 50 capsules per bottle and provides instructions to open capsules prior to administration without swallowing whole. Storage and usage warnings, along with the manufacturer location in Deer Park, IL, are also included.*

* 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.