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Kofal max power - Medication Information

Product NDC Code 55758-376
Drug Name

Kofal max power

Type Brand
Active Ingredients
Menthol, unspecified form 1.25 g/100g
Route TOPICAL
Dosage Form OINTMENT
Application Number part348
Labeler Name Pharmadel LLC
Packages
Package NDC Code Description
55758-376-05 142 g in 1 jar (55758-376-05)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient & Purpose Active ingredient Purpose Menthol 1.25% .................. External analgesic
Active ingredientPurpose
Menthol 1.25% ..................External analgesic

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 12 years of age and older: apply to affected area not more than 3 to 4 times daily children under 12 years of age: do not use, consult a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients alcohol, arnica montana flower, cannabis sativa (hemp) seed oil, camphor, carbomer 940, DMDM hydantoin, eucalyptus oil, isopropyl alcohol, nonoxynol-9, polysorbate 20, propylene glycol, tea tree oil, trolamine, 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.
Uses For the temporary relief of minor aches and pains of muscles and joints associated with: simple backache arthritis strains bruises sprains

Purpose

Information about the drug product’s indications for use.
Active ingredient Purpose Menthol 1.25% .................. External analgesic
Active ingredientPurpose
Menthol 1.25% ..................External analgesic

Spl product data elements

Usually a list of ingredients in a drug product.
Kofal Max Power Menthol NONOXYNOL-9 POLYSORBATE 20 TEA TREE OIL ISOPROPYL ALCOHOL CAMPHOR (SYNTHETIC) ARNICA MONTANA FLOWER CARBOMER 940 WATER DMDM HYDANTOIN ALCOHOL EUCALYPTUS OIL MENTHOL, UNSPECIFIED FORM MENTHOL, UNSPECIFIED FORM CANNABIS SATIVA SEED OIL PROPYLENE GLYCOL 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.
Principal Display Panel Kofal MP PDP

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.
Drug Facts Distributed by: Pharmadel LLC New Castle, DE 19720 +1-866-359-3478

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.
Do not apply on wounds or irritated skin bandage tightly

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 immediately.

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other information store between 59°- 86°F (15 - 30°C) do not use if clear seal over jar is broken, torn or missing

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 and ask doctor immediately if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breast-feeding, ask a health care professional before use.

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. Avoid contact with the eyes. Do not apply on wounds or irritated skin bandage tightly Stop use and ask doctor immediately 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 health care professional before use. Keep out of reach of children. If swallowed get medical help, or contact a Poison Control Center immediately.

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