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Manufacturer
Target Corporation | RAPID AID VIET NAM COMPANY LIMITED
Effective date
2025-11-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:17:33

Label at a glance#

ProductUp up
Active ingredientCAPSICUM, CAMPHOR (SYNTHETIC), LEVOMENTHOL
Label structure12 sections

Dosage and administration

Adults and children 12 years of age and older:apply to affected area; change patch 1 to 2 times daily Children under 12 years of age: consult a doctor before use How to Apply Clean and dry affected area Cut open pouch and remove patch Remove protective film and apply directly to area of pain Apply to affected area not more than 3 times daily. Do not leave on skin for more than a total of 8 hours per day Wash hands...

Storage and handling

This product may cause allergic reaction on some individuals Store in cool dry place away from direct sunlight Store at 15-30°C (59-86°F)

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Camphor 110mg +Menthol 33mg + Capsicum Extract 22mg

Use

INDICATIONS & USAGE SECTION

For temporary relief of pain

Warnings

WARNINGS SECTION

For external use only.

When using this product:

OTC - WHEN USING SECTION

Use only as directed

do not get into eyes or on mucous membranes. If contact occurs, rinse thoroughly with water

do not apply to wounds, damaged or irritated skin

do not bandage or cover with any type of wrap except clothing

do not use with a heating pad or apply external heat

do not use 1 hour prior to bathing or within 30 minutes after bathing

Stop use and ask a doctor if:

OTC - STOP USE SECTION

Condition worsens,

Severe skin irritation occurs

Pain persist for more than 7 days

Symptoms clear up and occur again within a few days.

If pregnant or breast feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older:apply to affected area; change patch 1 to 2 times daily

Children under 12 years of age: consult a doctor before use

How to Apply

Clean and dry affected area

Cut open pouch and remove patch

Remove protective film and apply directly to area of pain

Apply to affected area not more than 3 times daily. Do not leave on skin for more than a total of 8 hours per day

Wash hands with soap after applying patch

Reseal pouch containing unused patches

Children under 2 years of age: do not use, consult a physician

Other information

STORAGE AND HANDLING SECTION

This product may cause allergic reaction on some individuals

Store in cool dry place away from direct sunlight

Store at 15-30°C (59-86°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylamide/Sodium Acryloyldimethyltaurate Copolymer, Dihydroxyaluminum aminoacetate, DMDM hydantoin, Edetic acid, Glycerin, Laurocapram, Polyacrylic acid, Sodium polyacrylate, Tartaric acid, Titanium dioxide, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANELPACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1994328Capsicum extract 22 MG / levomenthol 33 MG / synthetic camphor 110 MG Medicated PatchPSN1
1994328Capsicum extract 22 MG / levomenthol 33 MG / synthetic camphor 110 MG Medicated PatchSCD1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CAPSICUM Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82442-745-05Up up5000 mg in 1 POUCHPATCH50001

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82442-74582442-745-05

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Up upPAIN RELIEF ADVANCED HYDROGEL PATCHESTarget Corporation44128b70-3172-ee37-e063-6294a90a705f2025-11-20WarningsExact identifier
ndc (package): 82442-745-05
ndc (product): 82442-745
ndc11 (package): 82442074505
spl id: 44128b70-3173-ee37-e063-6294a90a705f
spl set id: 44128b70-3172-ee37-e063-6294a90a705f

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.