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Lidoplus pain relief - Medication Information

Product NDC Code 70372-723
Drug Name

Lidoplus pain relief

Type Brand
Pharm Class Amide Local Anesthetic [EPC],
Amides [CS],
Antiarrhythmic [EPC],
Local Anesthesia [PE]
Active Ingredients
Lidocaine hydrochloride 40 mg/ml
Route TOPICAL
Dosage Form CREAM
RxCUI drug identifier 1010895
Application Number M017
Labeler Name Centura Pharmaceuticals, Inc
Packages
Package NDC Code Description
70372-723-01 1 tube in 1 box (70372-723-01) / 118 ml in 1 tube
70372-723-02 5 ml in 1 packet (70372-723-02)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients: Lidocaine HCl 4.00% Topical Anesthetic

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 two-years of age or older: Apply to affected area not more than three to four times daily. • Children under two-years of age: consult a physician.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Other Ingredients: Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Flower Extract, Boswellia Serrata Extract, C13-14 Isoparaffin, Cetyl Alcohol, Chondroitin Sulfate, Dimethyl Sulfone (MSM), Ethylhexylglycerin, Glucosamine Sulfate, Glyceryl Stearate, Glycerin, Hamamelis Virginiana (Witch Hazel) Extract, Laureth-7, PEG-100 Stearate, Phenoxyethanol, Polyacrylamide, Polysorbate-20, Stearic Acid.

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.
Indications: For the temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites and minor skin irritations.

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
LidoPlus Pain Relief LIDOCAINE HYDROCHLORIDE ALOE VERA LEAF WATER ARNICA MONTANA FLOWER INDIAN FRANKINCENSE C13-14 ISOPARAFFIN CETYL ALCOHOL ETHYLHEXYLGLYCERIN GLUCOSAMINE SULFATE GLYCERYL MONOSTEARATE GLYCERIN HAMAMELIS VIRGINIANA TOP LAURETH-7 PEG-100 STEARATE PHENOXYETHANOL POLYSORBATE 20 STEARIC ACID LIDOCAINE HYDROCHLORIDE LIDOCAINE LIDOCAINE HYDROCHLORIDE

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 Labeling: Label 2

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.
Drug Facts

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use in large quantities, particularly over raw surfaces or blistered areas.

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, consult physician.

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breast feeding, contact physician prior to use.

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. • Avoid contact with eyes. • If condition worsens or symptoms persist for more than seven days, discontinue use and consult physician. Keep out of reach of children. If swallowed, consult physician. Do not use in large quantities, particularly over raw surfaces or blistered areas. If pregnant or breast feeding, contact physician prior to use.

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