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Icy hot pro pain - Medication Information

Product NDC Code 41167-0074
Drug Name

Icy hot pro pain

Type Brand
Active Ingredients
Camphor (synthetic) 180 mg/1
Menthol 300 mg/1
Route TOPICAL
Dosage Form PATCH
RxCUI drug identifier 2393604
Application Number 505G(a)(3)
Labeler Name Chattem, Inc.
Packages
Package NDC Code Description
41167-0074-0 5 patch in 1 carton (41167-0074-0)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active i ngredient s Camphor 3% Menthol 5%

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: ■ remove backing from patch by firmly grasping both ends and gently pulling until backing separates in middle ■ carefully remove smaller portion of backing from patch and apply exposed portion of patch to affected area ■ once exposed portion of patch is positioned, carefully remove remaining backing to completely apply patch to affected area ■ apply to affected area not more than 3 to 4 times daily ■ wash hands after applying or removing patch. Throw away the patch by folding sticky ends together. ■ children under 12 years of age: ask a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients aluminum hydroxide, cellulose gum, disodium EDTA, glycerin, methyl acrylate/2-ethylhexyl acrylate copolymer, nonoxynol-30, polyacrylic acid, polysorbate 80, propylene glycol, silica, sodium polyacrylate, talc, tartaric acid, titanium dioxide, water Keep carton as it contains important information.

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 temporarily relieves minor aches and pains of muscles and joints associated with: ■ arthritis ■ simple backache ■ strains ■ sprains ■ bruises

Purpose

Information about the drug product’s indications for use.
Purpose Topical analgesic Topical analgesic

Spl product data elements

Usually a list of ingredients in a drug product.
Icy Hot Pro Pain Camphor and Menthol CAMPHOR (SYNTHETIC) CAMPHOR (SYNTHETIC) MENTHOL MENTHOL ALUMINUM HYDROXIDE CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED EDETATE DISODIUM ANHYDROUS GLYCERIN METHYL ACRYLATE ETHYLHEXYL ACETATE NONOXYNOL-30 POLYACRYLIC ACID (250000 MW) PROPYLENE GLYCOL POLYSORBATE 80 SILICON DIOXIDE SODIUM POLYACRYLATE (2500000 MW) TALC TARTARIC ACID TITANIUM DIOXIDE 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.
Principal Display Panel ICY HOT PRO PAIN RELIEF PATCH EXTRA STRENGTH WITH 2 PAIN RELIEVERS MENTHOL 5% CAMPHOR 3% CONTAINS 5 PATCHES IN 1 RESEALABLE POUCH ICY HOT PRO PAIN RELIEF PATCH EXTRA STRENGTH WITH 2 PAIN RELIEVERS MENTHOL 5% CAMPHOR 3% CONTAINS 5 PATCHES IN 1 RESEALABLE POUCH

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.
ICY HOT PRO PAIN PATCH Drug Facts

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 use ■ on wounds or on irritated or damaged skin ■ with a heating pad

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.

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 a doctor if ■ condition worsens or symptoms persist for more than 7 days ■ symptoms clear up and occur again within a few days ■ redness is present or excessive skin irritation occurs ■ you experience severe burning pain, swelling, or blistering where the product was applied

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product ■ use only as directed ■ do not bandage tightly ■ avoid contact with eyes and mucous membranes ■ do not expose the area to local heat or to direct sunlight ■ rare cases of serious burns have been reported with products of this type ■ a transient burning sensation may occur upon application but generally disappears in several days ■ avoid applying into skin folds

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breast-fee d ing, ask a health 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 Do not use ■ on wounds or on irritated or damaged skin ■ with a heating pad When using this product ■ use only as directed ■ do not bandage tightly ■ avoid contact with eyes and mucous membranes ■ do not expose the area to local heat or to direct sunlight ■ rare cases of serious burns have been reported with products of this type ■ a transient burning sensation may occur upon application but generally disappears in several days ■ avoid applying into skin folds Stop use and ask a doctor if ■ condition worsens or symptoms persist for more than 7 days ■ symptoms clear up and occur again within a few days ■ redness is present or excessive skin irritation occurs ■ you experience severe burning pain, swelling, or blistering where the product was applied If pregnant or breast-fee d ing, ask a health professional before use. Keep out of 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