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Icy hot lidocaine no-mess - Medication Information

Product NDC Code 41167-1711
Drug Name

Icy hot lidocaine no-mess

Type Brand
Pharm Class Amide Local Anesthetic [EPC],
Amides [CS],
Antiarrhythmic [EPC],
Local Anesthesia [PE]
Active Ingredients
Lidocaine hydrochloride 4 g/100g
Route TOPICAL
Dosage Form LIQUID
RxCUI drug identifier 1987647
Application Number M017
Labeler Name Chattem, Inc.
Packages
Package NDC Code Description
41167-1711-0 42.5 g in 1 bottle (41167-1711-0)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active i ngredient

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 a thin layer to affected area every 6 to 8 hours, not more than 3 to 4 times daily ■ massage until thoroughly absorbed into skin ■ wash hands thoroughly with soap and water after each use ■ children under 12 years of age: ask a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients acrylates/C10-30 alkyl acrylate crosspolymer, alcohol denat. (15%), aloe barbadensis leaf juice, aminomethyl propanol, C30-45 alkyl cetearyl dimethicone crosspolymer, caprylyl methicone, cetearyl alcohol, ceteth-20 phosphate, dicetyl phosphate, dimethicone, disodium EDTA, ethylhexylglycerin, glyceryl stearate, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, isohexadecane, methylparaben, polysorbate 60, steareth-2, steareth-21, water 333-104 Child-resistant packaging. Close cap tightly after use . 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.
Use for the temporary relief of pain

Purpose

Information about the drug product’s indications for use.
Purpose Lidocaine HCl 4%............................................................................................................................Topical anesthetic

Spl product data elements

Usually a list of ingredients in a drug product.
Icy Hot Lidocaine No-Mess LIDOCAINE HYDROCHLORIDE LIDOCAINE HYDROCHLORIDE LIDOCAINE LIDOCAINE HYDROCHLORIDE ANHYDROUS ALCOHOL ALOE VERA LEAF AMINOMETHYLPROPANOL C30-45 ALKYL CETEARYL DIMETHICONE CROSSPOLYMER CETETH-20 PHOSPHATE DIMETHICONE ETHYLHEXYLGLYCERIN HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) ISOHEXADECANE METHYLPARABEN POLYSORBATE 60 STEARETH-2 STEARETH-21 WATER CARBOMER INTERPOLYMER TYPE A (55000 CPS) EDETATE DISODIUM ANHYDROUS GLYCERYL MONOSTEARATE DIHEXADECYL PHOSPHATE CAPRYLYL TRISILOXANE CETOSTEARYL ALCOHOL

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 Lidocaine 4% IcyHot Max PRINCIPAL DISPLAY PANEL Lidocaine 4% IcyHot Max

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 H OT with LIDOCAINE CREAM (MAX) 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 ■ in large quantities ■ 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

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 Flammable ■ keep away from heat and open flame. Do not use ■ in large quantities ■ 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 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