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Lidocaine Hydrochloride

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Overview

What is CidalEaze?

CidalEaze (Lidocaine 3% Cream) is a topical anesthetic indicated for the relief of 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.



What does CidalEaze look like?



What are the available doses of CidalEaze?

Sorry No records found.

What should I talk to my health care provider before I take CidalEaze?

Sorry No records found

How should I use CidalEaze?

Anesthetic for relief of 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.

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


What interacts with CidalEaze?

Sorry No Records found


What are the warnings of CidalEaze?

Sorry No Records found


What are the precautions of CidalEaze?

Sorry No Records found


What are the side effects of CidalEaze?

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.


What should I look out for while using CidalEaze?

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.

For external use only. Not for ophthalmic use.


What might happen if I take too much CidalEaze?

Sorry No Records found


How should I store and handle CidalEaze?

StorageStore PROTONIX For Delayed-Release Oral Suspension and PROTONIX Delayed-Release Tablets at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) .Repackaged by:Cardinal HealthZanesville, OH 43701LUP39994060211L399940600112L7775G1113L32622760212L45542751214StorageStore PROTONIX For Delayed-Release Oral Suspension and PROTONIX Delayed-Release Tablets at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) .Repackaged by:Cardinal HealthZanesville, OH 43701LUP39994060211L399940600112L7775G1113L32622760212L45542751214StorageStore PROTONIX For Delayed-Release Oral Suspension and PROTONIX Delayed-Release Tablets at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) .Repackaged by:Cardinal HealthZanesville, OH 43701LUP39994060211L399940600112L7775G1113L32622760212L45542751214StorageStore PROTONIX For Delayed-Release Oral Suspension and PROTONIX Delayed-Release Tablets at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) .Repackaged by:Cardinal HealthZanesville, OH 43701LUP39994060211L399940600112L7775G1113L32622760212L45542751214StorageStore PROTONIX For Delayed-Release Oral Suspension and PROTONIX Delayed-Release Tablets at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) .Repackaged by:Cardinal HealthZanesville, OH 43701LUP39994060211L399940600112L7775G1113L32622760212L45542751214StorageStore PROTONIX For Delayed-Release Oral Suspension and PROTONIX Delayed-Release Tablets at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) .Repackaged by:Cardinal HealthZanesville, OH 43701LUP39994060211L399940600112L7775G1113L32622760212L45542751214StorageStore PROTONIX For Delayed-Release Oral Suspension and PROTONIX Delayed-Release Tablets at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) .Repackaged by:Cardinal HealthZanesville, OH 43701LUP39994060211L399940600112L7775G1113L32622760212L45542751214StorageStore PROTONIX For Delayed-Release Oral Suspension and PROTONIX Delayed-Release Tablets at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) .Repackaged by:Cardinal HealthZanesville, OH 43701LUP39994060211L399940600112L7775G1113L32622760212L45542751214StorageStore PROTONIX For Delayed-Release Oral Suspension and PROTONIX Delayed-Release Tablets at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) .Repackaged by:Cardinal HealthZanesville, OH 43701LUP39994060211L399940600112L7775G1113L32622760212L45542751214StorageStore PROTONIX For Delayed-Release Oral Suspension and PROTONIX Delayed-Release Tablets at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) .Repackaged by:Cardinal HealthZanesville, OH 43701LUP39994060211L399940600112L7775G1113L32622760212L45542751214CidalEaze (Lidocaine 3% Cream) is supplied as a white cream in: 16 oz. (453.65 g) jar, NDC 15455-9526-1


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Clinical Information

Chemical Structure

No Image found
Clinical Pharmacology

CidalEaze (Lidocaine 3% Cream) releases lidocaine from a mild acidic vehicle to stabilize the neuronal membrane by inhibiting the ionic fluxes required for initiation and conduction of impulses, thereby effecting local anesthetic action. A mild acidic vehicle lowers pH to increase protection against alkaline irritations and to provide a favorable environment for healing.

Lidocaine is chemically designated as acetamide, 2- (diethylamino)-N-(2,6-dimethylphenyl), and has the following structure.

Non-Clinical Toxicology
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.

For external use only. Not for ophthalmic use.

(Clinical Evaluation of Drug Interactions Conducted with Metformin Hydrochloride Tablets)

If irritation or sensitivity occurs or infection appears, discontinue use and institute appropriate therapy. CidalEaze (Lidocaine 3% Cream) should be used with caution in ill, elderly, debilitated patients and children who may be more sensitive to the systemic effects of lidocaine.

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.

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Reference

This information is obtained from the National Institute of Health's Standard Packaging Label drug database.
"https://dailymed.nlm.nih.gov/dailymed/"

While we update our database periodically, we cannot guarantee it is always updated to the latest version.

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Professional

Clonazepam Description Each single-scored tablet, for oral administration, contains 0.5 mg, 1 mg, or 2 mg Clonazepam, USP, a benzodiazepine. Each tablet also contains corn starch, lactose monohydrate, magnesium stearate, microcrystalline cellulose, and povidone. Clonazepam tablets USP 0.5 mg contain Yellow D&C No. 10 Aluminum Lake. Clonazepam tablets USP 1 mg contain Yellow D&C No. 10 Aluminum Lake, as well as FD&C Blue No. 1 Aluminum Lake. Chemically, Clonazepam, USP is 5-(o-chlorophenyl)-1,3-dihydro-7-nitro-2H-1,4-benzodiazepin-2-one. It is a light yellow crystalline powder. It has the following structural formula: C15H10ClN3O3 M.W. 315.72
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Interactions

Interactions

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