Lidocaine Hydrochloride and Hydrocortisone Acetate

FDA Drug Profile — Lidocaine Hydrochloride and Hydrocortisone Acetate

Drug Details

Generic Name
Lidocaine Hydrochloride and Hydrocortisone Acetate
Brand Names
Lidocaine Hydrochloride and Hydrocortisone Acetate
Application Number
Sponsor
Seton Pharmaceuticals
NDC Codes
5
Dosage Forms
GEL, CREAM
Routes
RECTAL, TOPICAL
Active Ingredients
HYDROCORTISONE ACETATE, LIDOCAINE HYDROCHLORIDE

Warnings

WARNINGS: For external use only. Not for ophthalmic use. Product, applicators and moist wipes could harm small children if chewed or swallowed. Keep product, moist wipes and applicators out of the reach of children. Methemoglobinemia Cases of methemoglobinemia have been reported in association with local anesthetic use. Although all patients are at risk for methemoglobinemia, patients with glucose-6-phosphate dehydrogenase deficiency, congenital or idiopathic methemoglobinemia, cardiac or pulmonary compromise, infants under 6 months of age, and concurrent exposure to oxidizing agents or their metabolites are more susceptible to developing clinical manifestations of the condition. If local anesthetics must be used in these patients, close monitoring for symptoms and signs of methemoglobinemia is recommended. Signs and symptoms of methemoglobinemia may occur immediately or may be delayed some hours after exposure and are characterized by a cyanotic skin discoloration and abnormal coloration of the blood. Methemoglobin levels may continue to rise; therefore, immediate treatment is required to avert more serious central nervous system and cardiovascular adverse effects, including seizures, coma, arrhythmias, and death. Discontinue [the use of this product] and any other oxidizing agents. Depending on the severity of the symptoms, patients may respond to supportive care, i.e., oxygen therapy, hydration. More severe symptoms may require treatment with methylene blue, exchange transfusion, or hyperbaric oxygen.