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OTC

Up up

lidocaine pain relief maximum strength patches · Up up is an amide local anesthetic (over-the-counter) containing lidocaine pain relief maximum strength patches, made by Target Corporation.

Type
Over the counter
Drug class
Amide Local Anesthetic
Route
Topical
Manufacturers
1

For temporary relief of pain.

Drug facts

Generic name
lidocaine pain relief maximum strength patches
Active ingredients
Lidocaine
Dosage forms
Patch
Label holder
Target Corporation
FDA application
M017
Label updated
11/20/2025

Active ingredients

(s) Lidocaine 4 % w/w

Purpose

Topical anesthetic

Uses

For temporary relief of pain.

Directions

Adults and children 12 years of age and older: apply to affected area; changes patch 1 to 2 daily. Children under 12 years of age: consult a doctor. Supervise children when they use this product How to apply: Clean and dry affected area Remove film from patch and apply directly to area of pain Apply 1 patch at a time to the affected area, not more than 3 to 4 times daily. Remove patch from the skin. Do not leave on skin for more than a total of 8 hours per day. Children under 12 years of age: do not use, consult a doctor.

Warnings

For external use only.

Do not use

More than 1 patch at a time If you are allergic to any ingredients of this product In large quantities, particularly over raw surface or blistered areas.

When using this product

Use only as directed Do not bandage tightly Avoid contact with eyes, mucous membranes or rashes If contact occurs, rinse thoroughly with water. Do not apply to wounds, damaged or irritation skin. Do not use with a heating pad such as electric heating pad, as this may result in excessive skin irritation or skin burn.

Stop use and ask a doctor

Condition worsens Severe skin irritation occurs Symptoms persist for more than 7 days Symptoms clear up and occur again within a few days

Pregnancy or breastfeeding

If pregnant or breastfeeding If pregnant or breastfeeding, ask a health professional before use.

Keep out of reach of children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Other information

Store between 15-30℃(59-86℉) Protect product from excessive moisture Avoid storing product in direct sunlight

Inactive ingredients

Acyclmide/Sodium Acryloyldimethyltaurate copolyme, Dihydroxyaluminum aminoacetetel, DMDM hydantoin, Edetic acid, Glycerin, Polyacrylic acid, Sodium polyacrylate, Tartaric acid, Titanium dioxide, Water

Forms and strengths

From the FDA NDC Directory · 1 product codes

Dosage formStrengthRouteNDCs
Patch4 g/100gtopical1

Manufacturers and labels

1 FDA label

  • Target CorporationShown hereM017 · Label 11/20/2025 · NDC 82442-744Full label

Related recalls

FDA drug recalls that name this drug or its active ingredient

All drug recalls

Up up: common questions

What is Up up used for?
For temporary relief of pain.
Is Up up a prescription drug?
No. Up up is sold over the counter (OTC) without a prescription.
Are there other products with the same active ingredient as Up up?
Yes. Other FDA-listed products with the same active ingredients include Pain Relief Patches, Burn Relief, LIDOCAINE PAIN RELIEF Gel-Patch, Lidocaine Numbing Cream.
Who makes Up up?
Target Corporation lists Up up with the FDA.

Source: U.S. Food and Drug Administration, openFDA drug label (SPL) and NDC Directory · Last updated 11/20/2025 · Label text is shown as published by the manufacturer. Not medical advice