Careland Kinesiology Dual Action + Pain Relieving Tape

Manufacturer
Planet (Anhui) Pharmaceutical Co., Ltd.
Effective date
2026-06-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-07-21 05:10:16

Label at a glance#

ProductCareland Kinesiology Dual Action Pain Relieving Tape
Active ingredientLIDOCAINE, MENTHOL, UNSPECIFIED FORM
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 starting at a corner Apply sticky side of patch to affected area Discard after single use Children under 12 years of age :  consult a physician.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Menthol 1%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

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 a 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 the patch.

Stop use and consult a doctor if

OTC - STOP USE SECTION

  • Condition worsens
  • Redness is present
  • Irritation develops
  • Symptom 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 professional 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 starting at a corner
  • Apply sticky side of patch to affected area
  • Discard after single 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

 Aluminum Silicate, Mineral Oil, Polyisobutylene, Propylene Glycol, Styrene-Isoprene-Styrene Block Copolymer, Terpene Resin.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label0Label0

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
75568-05075568-050-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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 Dual Action Pain Relieving TapeLIDOCAINEPlanet (Anhui) Pharmaceutical Co., Ltd.67e0b3c5-e88e-4c48-a1e8-39f502ac249d2026-06-18WarningsExact identifier
ndc (package): 75568-050-00
ndc (product): 75568-050
ndc11 (package): 75568005000
spl id: 5488fd8c-7ef5-22c2-e063-6394a90aff3c
spl set id: 67e0b3c5-e88e-4c48-a1e8-39f502ac249d

Reported adverse events (FAERS/openFDA)#

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