Product Elements:
Radiaura skin recovery lidocaine hcl - hydrocortisone acetate prezatide copper acetate green tea leaf cannabis sativa seed oil cetostearyl alcohol coco-caprylate/caprate hydrogenated jojoba oil, randomized arbutin levomenol indian frankincense rapeseed sterol shea butter calendula officinalis flower chitosan medium molecular weight (200-800 mpa.s) cucumber hyaluronate sodium tetrahydrodiferuloylmethane tetrahydrodemethoxydiferuloylmethane peg-100 stearate water sodium hydroxide sorbitan monostearate stearyl alcohol cetyl alcohol stearic acid lecithin, soybean phenoxyethanol polyglyceryl-3 diisostearate jojoba oil squalane tetrahydrobisdemethoxydiferuloylmethane lidocaine hydrochloride lidocaine lidocaine hydrochloride anhydrous hydrocortisone acetate hydrocortisone hydroxyethyl cellulose, unspecified tetrahexyldecyl ascorbate glyceryl monostearate glycerin coconut alkanes turmeric .alpha.-tocopherol, d- dextrose
Indications and Usage:
Indications: the product is used for the anti-inflammatory and anesthetic relief of redness, pain, itching, and discoloration due to inflammation and skin burns. for the relief of redness, pain, itching, discoloration, inflammation and mild skin burns associated with radiation. for use after radiation treatment, cosmetic procedures, sun exposure, and for inflammatory skin conditions.
Warnings:
Warnings: concerns related to adverse effects: methemoglobinemia: has been reported with local anesthetics; clinically significant methemoglobinemia requires immediate treatment along with discontinuation of the anesthetic and other oxidizing agents. onset may be immediate or delayed (hours) after anesthetic exposure. patients with g6pd deficiency, congenital or idiopathic methemoglobinemia, cardiac or pulmonary compromise, exposure to oxidizing agents or their metabolites, or infants <6 months of age are more susceptible and should be closely monitored for signs and symptoms of methemoglobinemia (including pale, gray, or blue-colored skin (cyanosis), headache, rapid pulse, shortness of breath, lightheadedness, fatigue). warnings: for external use only. not for ophthalmic use. keep out of reach of children. topical formulations of lidocaine may be absorbed to a greater extent through mucous membranes and abraded, fissured or irritated skin than through intact skin. product should not b
Read more...e ingested or applied into the mouth, inside of the nose or in the eyes. product should not be used in the ears. any situation where lidocaine penetrates beyond the tympanic membrane into the middle ear is contraindicated because of ototoxicity associated with lidocaine observed in animals when instilled in the middle ear. product should not come into contact with the eye or be applied into the eye because of the risk of severe eye irritation and the loss of eye surface sensation, which reduces protective reflexes and can lead to corneal irritation and possibly abrasion. if eye contact occurs, rinse out the eye immediately with saline or water and protect the eye surface until sensation is restored.
Dosage and Administration:
Dosage and administration: apply product to the affected area(s) twice daily or as directed by a physician. if the condition does not respond to repeated courses of product or should worsen, discontinue use and seek the advice of your physician. wash hands before and after application.
Contraindications:
Contraindications: product should not be used in patients with a history of sensitivity to any of its ingredients or adverse reactions to lidocaine or amide anesthetics, which usually do not cross-react with âcaineâ ester type anesthetics. if excessive irritation and significant worsening occur, discontinue use and seek the advice of your physician. product and topical lidocaine should be used cautiously in those with impaired liver function, as well as the very ill or very elderly and those with significant liver disease. product should be used with caution in patients receiving antiarrhythmic drugs of class i since the adverse effects are additive and generally synergistic. product is contraindicated for tuberculous or fungal lesions or skin vaccinia, varicella and acute herpes simplex. topical corticosteroids are contraindicated in those patients with a history of hypersensitivity to any of the components of the preparation.
Adverse Reactions:
Adverse reactions: during or immediately following application of product, there may be transient stinging or burning from open areas of skin, or transient blanching (lightening), or erythema (redness) of the skin.
Use in Pregnancy:
Use in pregnancy: teratogenic effects: pregnancy category c. reproduction studies have been performed for lidocaine in rats at doses up to 6.6 times the human dose and have revealed no evidence of harm to the fetus caused by lidocaine. there are, however, no adequate and well-controlled studies in pregnant women. animal reproduction studies are not always predictive of human response. general consideration should be given to this fact before administering lidocaine to women of childbearing potential, especially during early pregnancy when maximum organogenesis takes place. corticosteroids are generally teratogenic in laboratory animals when administered systemically at relatively low dosage levels. the more potent corticosteroids have been shown to be teratogenic after dermal application in laboratory animals. there are no adequate and well controlled studies in pregnant women on teratogenic effects from topically applied corticosteroids. therefore, topical corticosteroids should be us
Read more...ed during pregnancy only if the potential benefit justifies the potential risk to the fetus. drugs of this class should not be used extensively on pregnant patients, in large amounts, or for prolonged periods of time.
Pediatric Use:
Pediatric use: safety and efficacy in children have not been established.
Description:
Description: lidocaine is chemically designated as acetamide, 2-(diethylamino)-n-(2,6-dimethylphenyl), and has the following structure: hydrocortisone acetate has a chemical name pregn-4-ene-3, 20-dione, 21-(acetyloxy)-11, 17-dihydroxy-(11β)-, it has the following structural formula: radiaura skin recovery cream lidocaine hcl 3%- hydrocortisone acetate 0.5% each gram contains lidocaine hcl 30 mg, hydrocortisone acetate 5 mg. active ingredients: lidocaine hcl 3% (30 mg) hydrocortisone acetate 0.5% (5 mg). image description image description
Clinical Pharmacology:
Clinical pharmacology: mechanism of action: product releases lidocaine to stabilize the neuronal membrane by inhibiting the ionic fluxes required for initiation and conduction of impulses, thereby effecting local anesthetic action. hydrocortisone acetate provides relief of inflammatory and pruritic manifestations of corticosteroid responsive dermatoses. pharmacokinetics: lidocaine may be absorbed following topical administration to mucous membranes, its rate and extent of absorption depending upon the specific site of application, duration of exposure, concentration, and total dosage. in general, the rate of absorption of local anesthetic agents following topical application occurs most rapidly after intratracheal administration. lidocaine is also well-absorbed from the gastrointestinal tract, but little intact drug appears in the circulation because of biotransformation of the liver. lidocaine is metabolized rapidly by the liver, and metabolites and unchanged drug are excreted by the
Read more...kidneys. biotransformation includes oxidative n-dealkylation, ring hydroxylation, cleavage of the amide linkage, and conjungation. n-dealkylation, a major pathway of biotransformation, yields the metabolites monoethylglycinexylidide and glycinexylidide. the pharmacological/toxicological actions of these metabolites are similar to, but less potent than, those of lidocaine. approximately 90% of lidocaine administered is excreted in the form of various metabolites, and less than 10% is excreted unchanged. the primary metabolite in urine is a conjugate of 4-hydroxy-2, 6-dimethylaniline. the plasma binding of lidocaine is dependent of drug concentration, and the fraction bound decreases with increasing concentration. at concentrations of 1 to 4 g of free base per ml, 60 to 80 percent of lidocaine is protein bound. binding is also dependent on the plasma concentration of the alpha-1-acid-glycoprotein. lidocaine crosses the blood-brain and placental barriers, presumably by passive diffusion. studies of lidocaine metabolism following intravenous bolus injections have shown that the elimination half-life of this agent is typically 1.5 to 2 hours. because of the rapid rate at which lidocaine is metabolized, any condition that affects liver function may alter lidocaine kinetics. the half-life may be prolonged two-fold or more in patients with liver dysfunction. renal dysfunction does not affect lidocaine kinetics but may increase the accumulation of metabolites. factors such as acidosis and the use of cns stimulants and depressants affect the cns levels of lidocaine required to produce overt systemic effects. objective adverse manifestations become increasingly apparent with increasing venous plasma levels above 6 g free base per ml. in the rhesus monkey arterial blood levels of 18-21 g/ml have been shown to be the threshold for convulsive activity. the extent of percutaneous absorption of topical corticosteroids is determined by many factors including the vehicle, the integrity of the epidermal barrier, and the use of occlusive dressings. topical corticosteroids can be absorbed from normal intact skin. inflammation and/or other disease processes in the skin increase percutaneous absorption. occlusive dressings substantially increase the percutaneous absorption of topical corticosteroids. thus, occlusive dressings may be a valuable therapeutic adjunct for treatment of resistant dermatoses. once absorbed through the skin, topical corticosteroids are handled through pharmacokinetic pathways similar to systemically administered corticosteroids. corticosteroids are bound to plasma protein in varying degrees. corticosteroids are metabolized primarily in the liver and are then excreted by the kidneys. some of the topical corticosteroids and their metabolites are also excreted into the bile.
Mechanism of Action:
Mechanism of action: product releases lidocaine to stabilize the neuronal membrane by inhibiting the ionic fluxes required for initiation and conduction of impulses, thereby effecting local anesthetic action. hydrocortisone acetate provides relief of inflammatory and pruritic manifestations of corticosteroid responsive dermatoses.
Pharmacokinetics:
Pharmacokinetics: lidocaine may be absorbed following topical administration to mucous membranes, its rate and extent of absorption depending upon the specific site of application, duration of exposure, concentration, and total dosage. in general, the rate of absorption of local anesthetic agents following topical application occurs most rapidly after intratracheal administration. lidocaine is also well-absorbed from the gastrointestinal tract, but little intact drug appears in the circulation because of biotransformation of the liver. lidocaine is metabolized rapidly by the liver, and metabolites and unchanged drug are excreted by the kidneys. biotransformation includes oxidative n-dealkylation, ring hydroxylation, cleavage of the amide linkage, and conjungation. n-dealkylation, a major pathway of biotransformation, yields the metabolites monoethylglycinexylidide and glycinexylidide. the pharmacological/toxicological actions of these metabolites are similar to, but less potent than, t
Read more...hose of lidocaine. approximately 90% of lidocaine administered is excreted in the form of various metabolites, and less than 10% is excreted unchanged. the primary metabolite in urine is a conjugate of 4-hydroxy-2, 6-dimethylaniline. the plasma binding of lidocaine is dependent of drug concentration, and the fraction bound decreases with increasing concentration. at concentrations of 1 to 4 g of free base per ml, 60 to 80 percent of lidocaine is protein bound. binding is also dependent on the plasma concentration of the alpha-1-acid-glycoprotein. lidocaine crosses the blood-brain and placental barriers, presumably by passive diffusion. studies of lidocaine metabolism following intravenous bolus injections have shown that the elimination half-life of this agent is typically 1.5 to 2 hours. because of the rapid rate at which lidocaine is metabolized, any condition that affects liver function may alter lidocaine kinetics. the half-life may be prolonged two-fold or more in patients with liver dysfunction. renal dysfunction does not affect lidocaine kinetics but may increase the accumulation of metabolites. factors such as acidosis and the use of cns stimulants and depressants affect the cns levels of lidocaine required to produce overt systemic effects. objective adverse manifestations become increasingly apparent with increasing venous plasma levels above 6 g free base per ml. in the rhesus monkey arterial blood levels of 18-21 g/ml have been shown to be the threshold for convulsive activity. the extent of percutaneous absorption of topical corticosteroids is determined by many factors including the vehicle, the integrity of the epidermal barrier, and the use of occlusive dressings. topical corticosteroids can be absorbed from normal intact skin. inflammation and/or other disease processes in the skin increase percutaneous absorption. occlusive dressings substantially increase the percutaneous absorption of topical corticosteroids. thus, occlusive dressings may be a valuable therapeutic adjunct for treatment of resistant dermatoses. once absorbed through the skin, topical corticosteroids are handled through pharmacokinetic pathways similar to systemically administered corticosteroids. corticosteroids are bound to plasma protein in varying degrees. corticosteroids are metabolized primarily in the liver and are then excreted by the kidneys. some of the topical corticosteroids and their metabolites are also excreted into the bile.
Carcinogenesis and Mutagenesis and Impairment of Fertility:
Carcinogenesis, mutagenesis, and impairment of fertility: long-term animal studies have not been performed to evaluate the carcinogenic potential or the effect on fertility of topical corticosteroids. studies to determine mutagenicity with prednisolone and hydrocortisone have revealed negative results. studies of lidocaine in animals to evaluate the carcinogenic and mutagenic potential of the effect on fertility have not been conducted.
How Supplied:
How supplied: radiaura skin recovery cream (lidocaine hcl 3% - hydrocortisone acetate 0.5%) is supplied as a beige cream 3 oz. (85 g) tube - ndc 59088-432-07
Package Label Principal Display Panel:
Radiaura® skin recovery cream manufactured in the usa by: puretek corporation san fernando, ca 91340 for questions or information call toll-free: 877-921-7873 label