Package Label-principal Display Panel (600 mg/42.9 mg per 5 mL (75 mL Bottle))
This is a detailed description of the NDC 16714-294-01 Amoxicillin and Clavulanate Potassium Oral Suspension, with instructions for mixing, dosage information, storage requirements, and expiration details. The text provides information on the content of each 5 mL reconstituted suspension and highlights the need to keep medication out of reach of children. It includes information about phenylketonurics, color changes during the dosing period, and warning to use only if the inner seal is intact. The description also mentions the manufacturer, storage conditions, and expiration details. Remember to shake well before each use and refrigerate the suspension.*