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Lidocaine 4 percent - Medication Information

Product NDC Code 69420-6262
Drug Name

Lidocaine 4 percent

Type Brand
Pharm Class Amide Local Anesthetic [EPC],
Amides [CS],
Antiarrhythmic [EPC],
Local Anesthesia [PE]
Active Ingredients
Lidocaine hydrochloride 4 g/100g
Route TOPICAL
Dosage Form CREAM
RxCUI drug identifier 1010895
Application Number part348
Labeler Name SA3, LLC
Packages
Package NDC Code Description
69420-6262-1 120 g in 1 tube (69420-6262-1)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Lidocaine HCl 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 to 4 times a day children under 2 years ask a doctor
adults and children 2 years and olderapply externally to the affected area up to 3 to 4 times a day
children under 2 years ask a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Aqua (Deionized Water), Arnica Montana Flower Extract, Boswellia Serrata Extract, Cetearyl Alcohol, Chondroitin Sulfate, Dimethyl Sulfone (MSM), Ethylhexylglycerin, Glucosamine Sulfate, Glycerin, Glyceryl Stearate, C13-14 Isoparaffin, Isostearyl Palmitate, Laureth-7, PEG-100 Stearate, Phenoxyethanol, Polyacrylamide, Propylene Glycol, Sodium Polyacrylate, Stearic Acid, Triethanolamine.

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 sunburn minor scrapes minor burns insect bites minor skin irritations

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Lidocaine 4 Percent Lidocaine LIDOCAINE HYDROCHLORIDE LIDOCAINE LIDOCAINE HYDROCHLORIDE ANHYDROUS WATER ARNICA MONTANA FLOWER INDIAN FRANKINCENSE CETOSTEARYL ALCOHOL ETHYLHEXYLGLYCERIN GLUCOSAMINE SULFATE GLYCERIN GLYCERYL MONOSTEARATE C13-14 ISOPARAFFIN ISOSTEARYL PALMITATE LAURETH-7 PEG-100 STEARATE PHENOXYETHANOL PROPYLENE GLYCOL STEARIC ACID TROLAMINE CHONDROITIN SULFATE (BOVINE) DIMETHYL SULFONE POLYACRYLAMIDE (10000 MW) SODIUM POLYACRYLATE (2500000 MW)

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.
PRINCIPAL DISPLAY PANEL Lidocaine HCl 4% cream NDC 69420-6262-1 Topical Analgesic Cream 4.2 OZ ( 120 g ) SA3, LLC Table Description automatically generated

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 - L idocaine HCl 4% C ream SA3, LLC Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies. ---------- Lidocaine HCl 4% Topical Analgesic Cream ​Drug Facts

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.

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. If allergic reaction occurs or if redness, irritation, swelling, pain or other symptoms begin or increase.

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 Avoid contact with the eyes D o 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 May be applied under occlusive dressing. Store at 20-25°C (68-77°F); excursions permitted to 15-30°C (59-86°F). See USP Controlled Room Temperature.

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. When using this product Avoid contact with the eyes D o not use in large quantities, particularly over raw surfaces or blistered areas Stop use and ask a doctor If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. If allergic reaction occurs or if redness, irritation, swelling, pain or other symptoms begin or increase. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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