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Aspercreme with lidocaine foot pain creme - Medication Information

Product NDC Code 41167-0586
Drug Name

Aspercreme with lidocaine foot pain creme

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 CREAM
RxCUI drug identifier 1010895
Application Number M017
Labeler Name Chattem, Inc.
Packages
Package NDC Code Description
41167-0586-2 1 bottle, plastic in 1 carton (41167-0586-2) / 113 g in 1 bottle, plastic
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Lidocaine HCl 4%

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 over 12 years: apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period massage into painful area until thoroughly absorbed into skin children 12 years or younger: ask a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients water, SD alcohol 40 (10%), cetearyl alcohol, ceteth-20 phosphate, dimethicone, caprylyl methicone, dicetyl phosphate, glyceryl stearate, aloe barbadensis leaf juice, panthenol, tocopheryl acetate, magnesium ascorbyl phosphate, aminomethyl propanol, C30-45 alkyl cetearyl dimethicone crosspolymer, acrylates/C10-30 alkyl acrylate crosspolymer, ethylhexylglycerin, methylparaben, disodium EDTA, citric acid Child-resistant packaging. Close cap tightly after use.

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 temporarily relieves minor pain

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Aspercreme with Lidocaine Foot Pain Creme LIDOCAINE HYDROCHLORIDE LIDOCAINE HYDROCHLORIDE LIDOCAINE LIDOCAINE HYDROCHLORIDE ANHYDROUS WATER ALCOHOL CETOSTEARYL ALCOHOL CETETH-20 PHOSPHATE DIMETHICONE CAPRYLYL TRISILOXANE DIHEXADECYL PHOSPHATE GLYCERYL MONOSTEARATE ALOE VERA LEAF PANTHENOL ALPHA-TOCOPHEROL ACETATE MAGNESIUM ASCORBYL PHOSPHATE AMINOMETHYLPROPANOL CARBOMER INTERPOLYMER TYPE A (55000 CPS) ETHYLHEXYLGLYCERIN METHYLPARABEN EDETATE DISODIUM ANHYDROUS CITRIC ACID MONOHYDRATE

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 MAX STRENGTH Aspercreme WITH 4% LIDOCAINE PAIN RELIEF CREAM NET WT 4 OZ (113 g) MAX STRENGTH Aspercreme WITH 4% LIDOCAINE PAIN RELIEF CREAM NET WT 4 OZ (113 g)

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.
ASPERCREME LIDOCAINE FOOT CREME 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 large areas of the body or on cut, irritated or swollen skin on puncture wounds for more than one week without consulting a doctor

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 redness is present irritation develops symptoms persist for more than 7 days or clear up and occur again within a few days

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. Read and follow all directions and warnings on this carton. do not allow contact with the eyes and mucus membranes do not bandage tightly or apply local heat (such as heating pads) or a medicated patch to the area of use do not use at the same time as other topical analgesics

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breast-feeding, 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 large areas of the body or on cut, irritated or swollen skin on puncture wounds for more than one week without consulting a doctor When using this product use only as directed. Read and follow all directions and warnings on this carton. do not allow contact with the eyes and mucus membranes do not bandage tightly or apply local heat (such as heating pads) or a medicated patch to the area of use do not use at the same time as other topical analgesics Stop use and ask a doctor if condition worsens redness is present irritation develops 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 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