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Pain relief cream - Medication Information

Product NDC Code 84023-301
Drug Name

Pain relief 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 PASTE
Application Number M017
Labeler Name Shenzhen Yangan Technology Co., Ltd.
Packages
Package NDC Code Description
84023-301-01 1 bottle, plastic in 1 box (84023-301-01) / 60 g in 1 bottle, plastic
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Lidocaine 4%

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.
Adults and children 2 years of age and older: Apply to affected area notmore than 3 to 4 times daily. Children under 2 years of age: consult a doctor.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Aloe barbadebsis leaf juice (Aloe vera) Water Lecithin (Soybean) Propylene Glycol Tocopheryl Acetate Carbomer Menthol 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.
For the temporary relief of minor aches and pains of muscles and joints, associated with simple backache, arthritis, strains, bruises, and sprains.

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.
Pain Relief Cream Lidocaine LECITHIN, SOYBEAN LIDOCAINE LIDOCAINE ALOE WATER PROPYLENE GLYCOL ALPHA-TOCOPHEROL ACETATE MENTHOL CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE TROLAMINE

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.
label-3

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.
Pain Relief Cream

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.
on damaged or broken skin.

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.
If swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use

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.
rash or irritation develops and lasts. condition worsens, or if symptoms persist for more than 7 days or dearup and occur again within a few days.

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.
Avoid contact with the eyes. Do notbandage tightly.

Storage and handling

Information about safe storage and handling of the drug product.
Protect the product in this container from excessive heat and direct sun.

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.
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