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Amino rip muscle pain relief - Medication Information

Product NDC Code 54859-415
Drug Name

Amino rip muscle pain relief

Type Brand
Pharm Class Amide Local Anesthetic [EPC],
Amides [CS],
Antiarrhythmic [EPC],
Local Anesthesia [PE]
Active Ingredients
Lidocaine 4 mg/100ml
Route TOPICAL
Dosage Form LIQUID
RxCUI drug identifier 2197844
Application Number part348
Labeler Name LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION
Packages
Package NDC Code Description
54859-415-02 60 ml in 1 bottle (54859-415-02)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients Lidocaine HCl

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 over 12 years of age Apply generously to the affected area as needed every 6-8 hours, not to exceed 3 applications in a 24 hour period. Not for use in children under 12 years of age

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients camphor, glycerin, isopropyl alcohol, menthol, methylparaben, propylparaben, purified water, xantham 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.
Use Temporarily relieves minor pains

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.
Amino Rip Muscle Pain Relief Lidocaine HCl LIDOCAINE LIDOCAINE CAMPHOR (SYNTHETIC) GLYCERIN ISOPROPYL ALCOHOL MENTHOL METHYLPARABEN PROPYLPARABEN WATER XANTHAN GUM

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.
musclepain

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.

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 Do not use on large areas of the body or on cut, irritated or swollen skin on puncture wounds for more than one week without consulting a doctor. When using this product Use only as direct. Read and follow all directions and warnings on this label. Do not allow contact with eyes Do not bandage or apply local heat (such as heating pads) to the area of use. Stop use and ask doctor if Condition worsens Symptoms persist for more than 7 days or clear up and occur again within a few days If pregnant or breast feeding, ask a doctor before use. Keep out of the 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