Careland Kinesiology Pain Relieving Tape

Manufacturer
Planet (Anhui) Pharmaceutical Co., Ltd.
Effective date
2026-05-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-06-16 05:10:18

Label at a glance#

ProductCareland Kinesiology Pain Relieving Tape
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE
Label structure7 sections

Dosage and administration

Adults and children 12 years of age and over: Clean and dry affected area Carefully remove backing from patch starring at a comer Apply sticky side of patch to affected area Discard after singal use Children under 12 years of age: consult a physician.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 3.1% 
Menthol 6% 
Methyl Salicylate 10% 

Purpose

OTC - PURPOSE SECTION

Topical anesthetic

Use

INDICATIONS & USAGE SECTION

For temporary relief of pain

Warning

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

• On cut, irritated or swollen skin
• On puncture wounds
• For more than one week without consulting a doctor
• If you are allergic to any active or inactive ingredients

When using this product

OTC - WHEN USING SECTION

  • Use only as directed
  • Apply only to clean, dry and untreated skin
  • Read and follow all directions and warnings
  • Do not allow contact with the eyes
  • Do not use at the same time as other topical analgesics
  • Do not bandage tightly or apply local heat (such as heating pads) to the area of use
  • Do not microwave
  • Dispose of used patch in manner that always keeps product away from children and pets. Used patches still contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch

Stop use and consult a doctor if

OTC - STOP USE SECTION

  • Codition worsens
  • Redness is present
  • Irritation develops
  • Symptoms persist for more than 7 days or clear up and occur again within a few days
  • you experience signs of skin injury,such as pain,swelling or blistering where the product was applied

If pregnant or breastfeeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health profesional before use.

Keep out of reach of children and pets.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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 over:

  • Clean and dry affected area
  • Carefully remove backing from patch starring at a comer
  • Apply sticky side of patch to affected area
  • Discard after singal use
  • Children under 12 years of age:consult a physician.

Other information

SPL UNCLASSIFIED SECTION

  • Store in a clean, dry place outside of direct sunlight
  • Protect from excessive moisture

Inactive ingredients

INACTIVE INGREDIENT SECTION

A-tocopherol acetate,ESIS,Fumed Silica,Mineral Oil,Polyisobutylene,Terpene Resin,3,5-Di-tert-butyl-4-hydroxyhydrocinnamic acid neopentanetetrayl ester.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagePackage

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
75568-04975568-049-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
Careland Kinesiology Pain Relieving TapeCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATEPlanet (Anhui) Pharmaceutical Co., Ltd.35d24cfc-9d34-4fd7-9312-1673b092a3b92026-05-31WarningsExact identifier
ndc (package): 75568-049-00
ndc (product): 75568-049
ndc11 (package): 75568004900
spl id: 532870d8-d9cf-d5dd-e063-6294a90af46d
spl set id: 35d24cfc-9d34-4fd7-9312-1673b092a3b9

Reported adverse events (FAERS/openFDA)#

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