Lidopril XR

Name: Lidopril XR

Warnings

Application of Lidocaine and prilocaine cream to larger areas or for longer times than those recommended could result in sufficient absorption of lidocaine and prilocaine resulting in serious adverse effects (see Individualization of Dose).

Patients treated with class III anti-arrhythmic drugs (e.g., amiodarone, bretylium, sotalol, dofetilide) should be under close surveillance and ECG monitoring considered, because cardiac effects may be additive.

Studies in laboratory animals (guinea pigs) have shown that lidocaine and prilocaine cream has an ototoxic effect when instilled into the middle ear. In these same studies, animals exposed to lidocaine and prilocaine cream only in the external auditory canal, showed no abnormality. Lidocaine and prilocaine cream should not be used in any clinical situation when its penetration or migration beyond the tympanic membrane into the middle ear is possible.

Methemoglobinemia: Lidocaine and prilocaine cream should not be used in those rare patients with congenital or idiopathic methemoglobinemia and in infants under the age of twelve months who are receiving treatment with methemoglobin-inducing agents.

Very young patients or patients with glucose-6-phosphate dehydrogenase deficiencies are more susceptible to methemoglobinemia.

Patients taking drugs associated with drug-induced methemoglobinemia such as sulfonamides, acetaminophen, acetanilid, aniline dyes, benzocaine, chloroquine, dapsone, naphthalene, nitrates and nitrites, nitrofurantoin, nitroglycerin, nitroprusside, pamaquine, para-aminosalicylic acid, phenacetin, phenobarbital, phenytoin, primaquine, quinine, are also at greater risk for developing methemoglobinemia.

There have been reports of significant methemoglobinemia (20 to 30%) in infants and children following excessive applications of Lidocaine and prilocaine cream. These cases involved the use of large doses, larger than recommended areas of application, or infants under the age of 3 months who did not have fully mature enzyme systems. In addition, a few of these cases involved the concomitant administration of methemoglobin-inducing agents. Most patients recovered spontaneously after removal of the cream. Treatment with IV methylene blue may be effective if required.

Physicians are cautioned to make sure that parents or other caregivers understand the need for careful application of Lidocaine and Prilocaine Cream, to ensure that the doses and areas of application recommended in Table 2 are not exceeded (especially in children under the age of 3 months) and to limit the period of application to the minimum required to achieve the desired anesthesia.

Neonates and infants up to 3 months of age should be monitored for Met-Hb levels before, during, and after the application of Lidocaine and prilocaine cream, provided the test results can be obtained quickly.

How is Lidopril XR Supplied

Lidopril XR (idocaine 2.5% and Prilocaine 2.5% Cream, USP) with Occlusive Dressing Contains:

 Quantity  Size  Description
2 tubes   30 gram/tube  packed individually, in a child-resistant tube.
10   occlusive dressings  packed individually

NOT FOR OPHTHALMIC USE.

KEEP CONTAINER TIGHTLY CLOSED AT ALL TIMES WHEN NOT IN USE.

Storage: Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].

Rx only

Keep out of the reach of children.

NDC: 69336-826-01 

Distributed by:

Sterling-Knight Pharmaceuticals, LLC

Ripley, MS 38663

Lidopril XR 
lidocaine 2.5% and prilocaine 2.5% cream
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:69336-826
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LIDOCAINE (LIDOCAINE) LIDOCAINE 25 mg  in 1 g
PRILOCAINE (PRILOCAINE) PRILOCAINE 25 mg  in 1 g
Inactive Ingredients
Ingredient Name Strength
PEG-55 HYDROGENATED CASTOR OIL  
CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED)  
SODIUM HYDROXIDE  
WATER  
CARBOXYPOLYMETHYLENE  
Packaging
# Item Code Package Description
1 NDC:69336-826-01 1 TUBE in 1 CARTON
1 30 g in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA019941 08/16/2016
Labeler - Sterling-knight Pharmaceuticals,LLC (079556942)
Revised: 10/2016   Sterling-knight Pharmaceuticals,LLC
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