FDA.reportPublic FDA data

ARCTICZEN Pain Relief Knee Patch

Manufacturer
NUTRIOMO LABS PTE. LTD
Effective date
2024-07-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:58:25

Label at a glance#

ProductARCTICZEN Pain Relief Knee
Active ingredientCAMPHOR (SYNTHETIC), CAPSICUM, MENTHOL
Label structure9 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints.

Dosage and administration

Adults and children 12 years of age and older: clean and dry the affected area apply a patch at a time to the affected area; not more than 3 or 4 times daily to the affected area remove the patch from the skin after at most 8 hours of application. Children under 12 years of age:  consult a doctor.

Label contents#

Full prescribing information#

Active Ingredients(in each patch)

OTC - ACTIVE INGREDIENT SECTION

Camphor 10%

Capsicum Extract (containing 0.2% of capsaicin)

Menthol 15%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints.

Warnings

WARNINGS SECTION

For external use only. Avoid contact with the eyes.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days

Do not use

OTC - DO NOT USE SECTION

  • on wounds or damaged skin
  • do not bandage tightly

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older:

  • clean and dry the affected area
  • apply a patch at a time to the affected area; not more than 3 or 4 times daily to the affected area
  • remove the patch from the skin after at most 8 hours of application.

Children under 12 years of age: consult a doctor.

Other Information

SPL UNCLASSIFIED SECTION

  • Storing product in a clean, dry place outside of direct sunlight
  • protect product from excessive moisture
  • do not use if clear film is broken or missing.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Angelica Dahurica, Frankincense Resin (Ru Xiang), Ginger, Notoginseng Extract, Safflower, Wormwood.

Questions?

OTC - QUESTIONS SECTION

Call us at 1-800-856-5587

71856-516-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label1Label1Label2Label2

71856-516-30

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71856-51671856-516-02, 71856-516-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
FRANKINCENSER9XLF1R1WMIACT
GINGERC5529G5JPQIACT
SAFFLOWER4VBL71TY4YIACT
WORMWOODF84709P2XVIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB
CAPSICUM00UK7646FGACTIB
MENTHOLL7T10EIP3AACTIB

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
309b6628-4f47-7862-e063-6394a90aae882362dda5-317b-46b9-80cb-e13a952b1a9e2025-03-18WarningsExact identifier
spl set id: 2362dda5-317b-46b9-80cb-e13a952b1a9e

Reported adverse events (FAERS/openFDA)#

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