K19 RELIEF MENTHOL K19 LLC FDA Approved Indications: For the temporary relief of minor aches and pains of the muscles and joints associated with arthritis, simple backache, sprains, bruises and stains.
Generic: MENTHOL
Mfr: K19 LLC FDA OTC
FunFoxMeds box
Substance Menthol
Route
TOPICAL
Applications
M017
Product NDC
Package NDC

Drug Facts

Composition & Profile

Active Ingredients
Active Ingredient: Menthol 1.25% Topical Analgesic
Inactive Ingredients
Other Ingredients: Aqua (Deionized Water) Camphor Glycerin Glyceryl Laurate SD-Alcohol 40B.
Strengths
1.25 %
Treats Conditions
Indications For The Temporary Relief Of Minor Aches And Pains Of The Muscles And Joints Associated With Arthritis Simple Backache Sprains Bruises And Stains

Identifiers & Packaging

Container Type UNKNOWN
All Product Codes
UNII
L7T10EIP3A
Packaging

Package Labeling: Label

Package Descriptions
  • Package Labeling: Label

Overview

Indications: For the temporary relief of minor aches and pains of the muscles and joints associated with arthritis, simple backache, sprains, bruises and stains.

Indications & Usage

Indications: For the temporary relief of minor aches and pains of the muscles and joints associated with arthritis, simple backache, sprains, bruises and stains.

Dosage & Administration

Directions: Adults and children 2 years of age or older: Apply to affected area not more than 3 to 4 times daily. Chidlren under 2 years of age: consult a physician.

Warnings & Precautions
Warnings: For external use only. Avoid contact with eyes and mucous membranes. If symptoms persist for more than 7 days, discontinue use and consult physician. Keep Out of reach of children. If swallowed, consult physician. Do not apply to wounds or damaged skin. Do not bandage tightly. If pregnant or breast feeding, contact physician prior to use.
Purpose

Topical Analgesic

Keep Out of Reach of Children

Keep Out of reach of children. If swallowed, consult physician. Do not apply to wounds or damaged skin. Do not bandage tightly.


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