Sign In

Save up to 80% by drug discount in your pharmacy with "Pharmacy Near Me - National Drug Discount Card"

You can scan QR Code(just open camera on your phone/scan by application) from the image on prescription drug discount card to save it to your mobile phone. Or just click on image if you're on mobile phone.

View Generic:
View Brand:

Up and up lidocaine pain relief - Medication Information

Product NDC Code 11673-744
Drug Name

Up and up lidocaine pain relief

Type Brand
Pharm Class Amide Local Anesthetic [EPC],
Amides [CS],
Antiarrhythmic [EPC],
Local Anesthesia [PE]
Active Ingredients
Lidocaine 560 mg/1
Route PERCUTANEOUS, TOPICAL, TRANSDERMAL
Dosage Form PATCH
Application Number M017
Labeler Name Target Corporation
Packages
Package NDC Code Description
11673-744-91 6 pouch in 1 carton (11673-744-91) / 1 patch in 1 pouch
Check if available Online

Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Lidocaine 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 12 years of age and over: • clean and dry affected area • remove film from patch and apply to the skin (see illustration) • apply 1 patch at a time to affected area, not more than 3 to 4 times daily • remove patch from the skin after at most 8 hours of application Children under 12 years of age: consult a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients carboxymethylcellulose sodium, dihydroxyaluminum aminoacetate, edetate disodium, glycerin, kaolin, methylparaben, polyacrylic acid, polyvinyl alcohol, propylene glycol, propylparaben, purified water, sodium polyacrylate, sodium polyacrylate starch, sorbitol solution, tartaric acid, urea

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 temporary relief of 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.
up and up lidocaine pain relief lidocaine LIDOCAINE LIDOCAINE CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED DIHYDROXYALUMINUM AMINOACETATE EDETATE DISODIUM GLYCERIN KAOLIN METHYLPARABEN POLYVINYL ALCOHOL, UNSPECIFIED PROPYLENE GLYCOL PROPYLPARABEN WATER SORBITOL TARTARIC ACID UREA

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 Compare to active ingredient in Salonpas® & Aspercreme® Lidocaine Patch up to 8 hours maximum strength lidocaine pain-relief patches 4% lidocaine/topical anesthetic desensitizes aggravated nerves in back, neck, shoulders, knees and elbows for temporary relief of pain numbing unscented 6 PATCHES 31 15/16 IN x 5 1/2 IN (10 cm x 14 cm) EACH 7u2-uw-lidocaine-pain-relief-patches

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 • more than 1 patch at a time • on wounds or damaged skin • with a heating pad • if you have ever had an allergic reaction to this product or any of its ingredients

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 (1-800-222-1222).

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions? Call 1-888-547-7400

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 • localized skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering • conditions worsen • symptoms persist for more than 7 days • symptoms 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 • avoid contact with the eyes, mucous membranes or rashes • do not bandage tightly

Pregnancy or breast feeding

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

Storage and handling

Information about safe storage and handling of the drug product.
Other information • avoid storing product in direct sunlight • protect product from excessive moisture • store at 20-25°C (68-77°F)

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 • more than 1 patch at a time • on wounds or damaged skin • with a heating pad • if you have ever had an allergic reaction to this product or any of its ingredients When using this product • use only as directed • avoid contact with the eyes, mucous membranes or rashes • do not bandage tightly Stop use and ask a doctor if • localized skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering • conditions worsen • symptoms persist for more than 7 days • symptoms 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 (1-800-222-1222).

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