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Meijer pain relief - Medication Information

Product NDC Code 79481-1087
Drug Name

Meijer pain relief

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 GEL
RxCUI drug identifier 1010077
Application Number part348
Labeler Name Meijer
Packages
Package NDC Code Description
79481-1087-2 71 g in 1 bottle (79481-1087-2)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Lidocaine HCl 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.
Clean affected area before applying product. Adults and children 12 years of age and older, apply to the affected area not more than 3 to 4 times daily. Children under 12 years old ask a doctor.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Acrylates/C10-30 alkyl acrylate crosspolymer, alcohol denat., aloe barbadensis leaf extract, aminomethyl propanol, C30-45 alkyl cetearyl dimehticone crosspolymer, carpylyl methicone, cetearyl alcohol, ceteth-20 phosphate, dicetyl phosphate, dimethicone, disodium EDTA, ethylhexylglycerin, glyceryl stearate, methylparaben, steareth-21, water.

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 pain.

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Meijer Pain Relief Lidocaine HCl 4% DIMETHICONE 200 CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) ALCOHOL AMINOMETHYLPROPANOL C30-45 ALKYL CETEARYL DIMETHICONE CROSSPOLYMER WATER CETOSTEARYL ALCOHOL LIDOCAINE HYDROCHLORIDE LIDOCAINE LIDOCAINE HYDROCHLORIDE ANHYDROUS CETETH-20 PHOSPHATE ALOE VERA LEAF DIHEXADECYL PHOSPHATE CAPRYLYL TRISILOXANE METHYLPARABEN EDETATE DISODIUM ETHYLHEXYLGLYCERIN GLYCERYL MONOSTEARATE STEARETH-21

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

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.

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. Flammable-- Do not use while smoking or near heat or flame. When using this product avoid contact with eyes, do not apply to wounds or damaged skin, and do not bandage tightly. Stop use and ask a doctor if condition worsens, if symptoms persist for more than 7 days or clear up and occur again within a few days, redness or irritation develops.

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