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| Product NDC Code | 72602-002 | ||||
|---|---|---|---|---|---|
| Drug Name | Mentho patch cool |
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| Type | Brand | ||||
| Active Ingredients |
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| Route | TOPICAL | ||||
| Dosage Form | PATCH | ||||
| Application Number | M017 | ||||
| Labeler Name | THE EGYPTIAN SAUDI CO FOR MEDICAL MANUFACTURING MASCOMID | ||||
| Packages |
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| Check if available Online | Get Medication Prices online with Discount |
Active ingredient
A list of the active, medicinal ingredients in the drug product.Active ingridient section Menthol,Camphor,Methyl salicylate
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 3 years of age and older: apply to affected area not more than 3 to 4 times daily. Children under 3 years of age: consult doctor.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.INACTIVE INGREDIENT SECTION Glycerin ,Sodium poly acryl ate ,Aluminum chloride hex hydrate 2 , Anhydrous citric acid ,Tartaric acid 1 ,Poly sorbate -80 (tween 80) 0.5 ,Isopropyl myristate alcohol 2.5 ,Car boxy methyl cellulose (CMC) 2 EDETA 0.5 ,Polyvinyl pyrolidone(PVP-K90) 3 ,Water 48.35 ,titanium dioxide 0.05,ACRYLATE/ C10-30 ALKYL ACRYLATE,cross polymer
Purpose
Information about the drug product’s indications for use.Purpose For the temprorary releif of minor aches and pains of musceles and joints associated with simple backache, arthritis,strainsand sprains
Spl product data elements
Usually a list of ingredients in a drug product.Mentho patch cool Menthol GLYCERIN SODIUM POLYACRYLATE (2500000 MW) ALUMINUM CHLORIDE ANHYDROUS CITRIC ACID MONOHYDRATE TARTARIC ACID POLYSORBATE 80 ISOPROPYL MYRISTATE CARBOXYMETHYLCELLULOSE SODIUM (0.9 CARBOXYMETHYL SUBSTITUTION PER SACCHARIDE; 600 MPA.S AT 2%) EDETATE DISODIUM POLYACRYLIC ACID (800000 MW) TITANIUM DIOXIDE WATER CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) MENTHOL MENTHOL
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.Product label image description image description
Ask doctor
Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.Stop use and ask doctor If condition worsens If symptoms persist more than 7 days or clear up and occur again with a few days
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, get medical help or contact a Poison Control Center right away
Storage and handling
Information about safe storage and handling of the drug product.storage store in cool dry place avoid direct sunlight.
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 When Using this Product Avoid contact with eyes Do not apply to open wounds, or to damaged skin Do not bandage tightly.
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