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LidaMantle

Last reviewed on RxList: 11/29/2016
Drug Description

LidaMantle® Cream
(lidocaine HCl 3%) In an AcidMantle Vehicle

DESCRIPTION

Contains lidocaine HCl 3% in a compatible AcidMantle vehicle adjusted to the pH range for normal skin. Lidocaine is chemically designated as acetamide, 2-(diethylamino)-N-(2,6-dimethylphenyl), and has the following structure:

LidaMantle® Cream (Lidocaine HCl) Structural Formula Illustration

C14H22N2O       Mol. wt. 234.34

Each gram of LidaMantle® Cream contains Lidocaine HCl 30 mg, Aluminum Sulfate, Calcium Acetate, Cetyl Alcohol, Glycerin, Light Mineral Oil, Methylparaben, Petrolatum, Polysorbate 60, Propylparaben, Purified Water, Sodium Hydroxide, Sorbitan Stearate, Stearic Acid, and Stearyl Alcohol.

Each mL of LidaMantle® Lotion contains Lidocaine HCl 30 mg, Aluminum Sulfate, Calcium Acetate, Cetyl Alcohol, Glycerin, Light Mineral Oil, Methylparaben, Petrolatum, Polysorbate 60, Propylparaben, Purified Water, Sodium Hydroxide, Sorbitan Stearate, Stearic Acid, and Stearyl Alcohol.

For Consumers

What are the possible side effects of lidocaine topical?

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

Stop using lidocaine topical and call your doctor at once if you have any of these serious side effects:

  • uneven heartbeats;
  • drowsiness, confusion;
  • tremors, seizure (convulsions); or
  • blurred vision.

Less serious side effects include:

  • mild irritation, redness, or swelling where the medication is applied; or
  • numbness in places where the medicine is accidentally...
Indications & Dosage

INDICATIONS

Pruritus, pruritic eczemas, abrasions, minor burns, insect bites, pain, soreness and discomfort due to pruritus ani, pruritus vulvae, hemorrhoids, anal fissures, and similar conditions of the skin and mucous membranes.

DOSAGE AND ADMINISTRATION

Apply a thin film to the affected area two or three times daily or as directed by a physician.

HOW SUPPLIED

LidaMantle® Cream

1 oz. (28.35 g) tube NDC 10337-700-52
3 oz. (85 g) tube NDC 10337-700-19

LidaMantle® Lotion

177 mL bottle NDC 10337-705-10

KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

Store at controlled room temperature 15°-30° C (59°-86° F).

Protect from freezing.

Mfd. for: Doak Dermatologics, A Subsidiary Of Bradley Pharmaceuticals, Inc., 383 Route 46 West Fairfield, NJ 07004-2402 USA. Mfd. by: Groupe Parima, Inc. Montreal, QC H4S 1X6 Canada. Revised -0305

Side Effects & Drug Interactions

SIDE EFFECTS

During or immediately after treatment, the skin at the site of treatment may develop erythema or edema or may be the locus of abnormal sensation.

DRUG INTERACTIONS

No information provided.

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Report Problems to the Food and Drug Administration

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

Warnings & Precautions

WARNINGS

For external use only. Not for ophthalmic use.

PRECAUTIONS

If irritation or sensitivity occurs, or infection appears, discontinue treatment and institute appropriate therapy. LidaMantle® should be used with caution in ill, elderly, debilitated patients and children who may be more sensitive to the systemic effects of lidocaine.

Carcinogenesis, mutagenesis, and impairment Of fertility

Studies of lidocaine in animals to evaluate the carcinogenic and mutagenic potential of the effect on fertility have not been conducted.

Use In Pregnancy

Teratogenic Effects: Pregnancy Category B Reproduction studies have been performed 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 wellcontrolled 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.

Nursing Mothers

It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when this drug is administered to a nursing mother.

Pediatric Use

Dosage in pediatric patients would be reduced commensurate with age, body weight and physical condition.

Overdosage & Contraindications

OVERDOSE

No information provided.

CONTRAINDICATIONS

Traumatized mucosa, secondary bacterial infection of the area of proposed application and known hypersensitivity to any of the components. Lidocaine is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type.

Clinical Pharmacology

CLINICAL PHARMACOLOGY

Mechanism Of Action

LidaMantle® Cream and LidaMantle® Lotion release lidocaine which stabilizes the neuronal membrane by inhibiting the ionic fluxes required for initiation and conduction of impulses, thereby effecting local anesthetic action. AcidMantle vehicle lowers pH to increase protection against alkaline irritants and to provide a favorable environment for healing.

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 in 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 conjugation. 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 on 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 threshold for convulsive activity.

Medication Guide

PATIENT INFORMATION

No information provided. Please refer to the WARNINGS and PRECAUTIONS sections.

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