Sodium Oxybate Solution
Product Images NDC 0054-9628

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Sodium Oxybate (NDC 0054-9628). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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

Figure C (Figure C)

Illustration showing how to open a bottle of sodium oxybate oral solution with a tamper evident band. The diagram highlights the tamper evident band on the bottle cap and the steps for removing the cap, including lifting and twisting actions.*

FDA Label Image

Figure D (Figure D)

An instructional illustration showing a hand attaching a syringe to a bottle labeled as sodium oxybate oral solution. The image includes two inset close-ups comparing an incorrectly and correctly inserted syringe on the bottle's neck, emphasizing proper syringe attachment for correct use.*

FDA Label Image

Figure E (Figure E)

Illustration showing a measuring syringe with a plunger attached to a bottle labeled Sodium Oxybate Oral Solution. The diagram demonstrates how to draw the solution from the bottle by pulling the plunger upward.*

FDA Label Image

Figure F And Figure G (Figure F And G)

An instructional diagram showing proper use of a dosing syringe to measure sodium oxybate oral solution. The illustration depicts hands holding a bottle labeled "Sodium Oxybate Oral Solution" with a syringe attached at the top. Insets detail the liquid level inside the syringe, marked with gram measurements and indicating an air space above the liquid.*

FDA Label Image

Figure H (Figure H)

An instructional illustration showing two hands preparing an oral liquid dose. One hand holds an open bottle, while the other hand draws liquid from the bottle with a syringe. The syringe is partially inserted into the bottle, with an arrow indicating a turning or pressing motion on the syringe plunger. This diagram is consistent with administering sodium oxybate oral solution.*

FDA Label Image

Figure I And Figure J (Figure I And J)

An instructional diagram showing how to open a child-resistant cap on a medication bottle. One image depicts hands holding the cap with a 'Hold Tab Down' and 'Turn' instruction, while the other shows the cap in the non-child resistant open position on the bottle.*

FDA Label Image

Chemical Structure (Image 01)

Chemical structure of sodium oxybate, showing the sodium ion (Na+), a carboxylate group, and a butane backbone with hydroxyl group, depicting the molecular arrangement of this oral solution active ingredient.*

FDA Label Image

Bottle Label (Image 02)

Label for Sodium Oxybate Oral Solution 0.5 g/mL by Hikma Pharmaceuticals USA Inc. The label indicates this 180 mL oral solution is prescription only and must be diluted before use. It includes warnings to keep out of reach of children and instructions for pharmacists to dispense an enclosed Medication Guide. Storage at 25°C (77°F) is recommended.*

FDA Label Image

Figure A (Image 03)

Instructional illustrations for sodium oxybate oral solution showing a medication guide booklet, two pharmacy containers with child-resistant caps labeled with directions to hold tab down and turn, a dosing syringe marked with volume measurements, and a hand pouring water into a 1/4 cup measuring cup for dilution. A note states the measuring cup and water for dilution are not provided with the prescription.*

FDA Label Image

Figure B (Image 04)

An instructional illustration showing hands opening a safety cap on a bottle. The cap has instructions to 'HOLD TAB DOWN' and 'TURN,' indicating a child-resistant push-and-turn mechanism to open the container.*

* 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.