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Pharmacys prescription analgesic gel - Medication Information

Product NDC Code 72197-001
Drug Name

Pharmacys prescription analgesic gel

Type Brand
Active Ingredients
Menthol 1 g/100g
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 1039043
Application Number part346
Labeler Name American Consumer Products Corp
Packages
Package NDC Code Description
72197-001-08 227 g in 1 bottle, plastic (72197-001-08)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Active Ingredient: Menthol 1%

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.
Dosage & Administration Directions - adults and childrent 2 years of age and older: apply to affected area not more than 3 to 4 times daily - children under 2 years of age: do not use, consult a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Inactive Ingredients carbomer, isopropyl alcohol, nonyl phenyl polyoxyethylene ether, camphor, kathon CG, FD&C blue no. 1, triethanolamine, 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.
Indications & Usage Section Uses: For the temporary relief of minor aches and pains of muscles and joints associated with - simple backache - arthritis - strains - bruses - sprains When using this product - avoid contact with eyes - do not bandage tightly - do not apply to wounds or damaged skin - do not use with heating pads or other heating devices

Purpose

Information about the drug product’s indications for use.
Purpose Purpose: Pain relieving gel

Spl product data elements

Usually a list of ingredients in a drug product.
Pharmacys Prescription Analgesic Gel Menthol MENTHOL MENTHOL ISOPROPYL ALCOHOL CAMPHOR, (-)- CARBOMER 940 METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTURE 2,2',3,3',4,4',5,5',6-NONACHLORODIPHENYL ETHER TRIETHANOLAMINE LAURYL SULFATE TROLAMINE WATER

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.
Pharmacy's Prescription 8 OZ Ice Cold Analgesic Gel Pharmacys Prescription 8 OZ Ice Cold Analgesic

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 Keep our of reach of children. If swallowed get medical help or contact a Poison Control Center immediately.

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 Stop use and ask doctor if - condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.

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 Warnings: 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