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Lidocaine 4% topical anesthetic cream - Medication Information

Product NDC Code 83720-523
Drug Name

Lidocaine 4% topical anesthetic cream

Type Brand
Pharm Class Amide Local Anesthetic [EPC],
Amides [CS],
Antiarrhythmic [EPC],
Local Anesthesia [PE]
Active Ingredients
Lidocaine 4 g/100g
Route TOPICAL
Dosage Form CREAM
RxCUI drug identifier 1421893
Application Number M017
Labeler Name Oncor Pharmaceuticals
Packages
Package NDC Code Description
83720-523-01 1 tube in 1 carton (83720-523-01) / 30 g in 1 tube
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Drug Facts Active Ingredients Lidocaine 4% w/w

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions Adults and children 2 years and older: apply externally to the affected area up to 3-4 times daily. Children under 2 years of age: consult a physician.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Cetyl alcohol, Citric acid, Glycerin, Glyceryl stearate SE, Mineral oil, PEG-100 stearate, Phenoxyethanol, Purified water, Stearyl alcohol, White petrolatum, Xanthan gum.

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses Temporarily relieves pain and itching due to: Minor cuts Minor scrapes Sunburn Minor burns Minor skin irritations Insect bites

Purpose

Information about the drug product’s indications for use.
Purpose Topical Anesthetic

Spl product data elements

Usually a list of ingredients in a drug product.
Lidocaine 4% Topical Anesthetic Cream Lidocaine 4% CETYL ALCOHOL CITRIC ACID ACETATE MINERAL OIL WATER WHITE PETROLATUM GLYCERIN GLYCERYL STEARATE SE PEG-100 STEARATE PHENOXYETHANOL STEARYL ALCOHOL XANTHAN GUM LIDOCAINE LIDOCAINE

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Package Label ONCOR PHARMACEUTICALS NDC 83720- 523 -01 Lidocaine 4% Cream Topical Anesthetic Cream For External Use Only Not For Ophthalmic Use This product contains child-resistant packaging. To open, push down on the cap of the tube while turning and lift off. NET WT. 1.05 OZ. (30 gm) ONCOR PHARMACEUTICALS NDC 83720- 523 -01 Lidocaine 4% Cream Topical Anesthetic Cream For External Use Only Not For Ophthalmic Use This product contains child-resistant packaging. To open, push down on the cap of the tube while turning and lift off. NET WT. 1.05 OZ. (30 gm) Carton Tube

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Lidocaine 4% Cream See crimp of tube or carton for lot and exp. date. RETAIN CARTON FOR COMPLETE DRUG FACTS.

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
Stop use and ask a doctor if Allergic reaction occurs. Condition worsens or does not improve within 7 days. Symptoms clear up and return within a few days. Redness, irritation, swelling, pain or other symptoms begin or increase.

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away. You may report side effects by calling Oncor Pharmaceuticals (9 a.m. to 5 p.m. EST), at 1-443-876-7900 or FDA at 1-800-FDA-1088.

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product Do not use in or near the eyes. Do not use in large quantities, particularly over raw surfaces or blistered areas.

Storage and handling

Information about safe storage and handling of the drug product.
Other information Store at USP controlled room temperature 20°-25°C (68°-77°F). Manufactured In USA For : ONCOR PHARMACEUTICALS 8815 Center Park Dr Suite 430 Columbia Maryland 21045 Rev. 05/24

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings For external use only.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API