K-Power Patch

Manufacturer
BCT
Effective date
2023-04-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:55:09

Label at a glance#

ProductK-Power Patch
Active ingredientLITHOSPERMUM ERYTHRORHIZON WHOLE, CAPSAICIN, XANTHIUM STRUMARIUM LEAF, EUCOMMIA ULMOIDES WHOLE, HARPAGOPHYTUM PROCUMBENS WHOLE, ACHYRANTHES BIDENTATA WHOLE
Label structure11 sections

Indications and uses

temporarity relieves the minor aches and pains of muscles and joints associated with: ■■simple backache ■ arthritis ■ strains ■ uruises ■ sprains

Dosage and administration

■ use only as directed ■ adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily ■ children under 12 years of age: ask a doctor

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Achyranthes bidentata Extract 3%
Lithospermum erythrorhizon S.et Z Extract 3%
Xanthium strumarium L Extract 2%
Eucomniia ulmoides Extract 2%
Harpagophytum prostrate 1%
Capsaicin 0.4%

Purposes

OTC - PURPOSE SECTION

Achyranthes bidentata Extract 3% --------------------------Topical analgesic
Lithospermum erythrorhizon S.et Z Extract 3% -----------Topical analgesic
Xanthium strumarium L Extract 2% -------------------------Topical analgesic
Eucomniia ulmoides Extract 2% ----------------------------Topical analgesic
Harpagophytum prostrate 1% --------------------------------Topical analgesic
Capsaicin 0.4% ----------------------------------------------- Topical analgesic

Uses

INDICATIONS & USAGE SECTION

temporarity relieves the minor aches and pains of muscles and joints associated with:
■■simple backache ■ arthritis ■ strains ■ uruises ■ sprains

Warnings

WARNINGS SECTION

For external use only

Warnings

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Warnings

OTC - STOP USE SECTION

Stop use and ask a doctor if
■ condition worsens or symptoms persist for more than 7days
■ symptoms clear up and occur again within a few days
■ excessive skirt irritation occurs

Warnings

OTC - WHEN USING SECTION

When using this product
■ avoid contact with eyes or mucous membranes
■ do not bandage tightly

Warnings

OTC - DO NOT USE SECTION

Do not use
■ on wounds or damage skin ■ with a healing pad
■ on a child under 12 years of age with arthritiS-llke conditions
Ask a doctor before use if you have redness over the affected area

Directions

DOSAGE & ADMINISTRATION SECTION

■ use only as directed
■ adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily
■ children under 12 years of age: ask a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Tourmaline, Surfactant(SR-10), n-Butyl acrylate Methylmethacrylate Copolymer

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

K Power PatchK Power Patch

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
473d070d-1c38-488e-b991-c4d1bf45aab8Product name120210201

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83404-301-012024-07-30C16284748780-11030e365-61f2-111a-e063-dadaa90a10e283404-301 K-Power Patch
83404-301-012024-01-30C16284748780-11030e365-61f2-111a-e063-dadaa90a10e283404-301 K-Power Patch

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83404-301-01K-Power Patch85 mm in 1 PATCHPATCH851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83404-301K-POWER PATCH (ACHYRANTHES BIDENTATA EXTRACT, ACHYRANTHES BIDENTATA EXTRACT,) PATCH [BCT]11 package rows20230601_f942fa8e-3c4d-e857-e053-6394a90a4a65.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83404-30183404-301-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
f942fa8e-3c4e-e857-e053-6394a90a4a65f942fa8e-3c4d-e857-e053-6394a90a4a652023-04-13WarningsExact identifier
spl id: f942fa8e-3c4e-e857-e053-6394a90a4a65
spl set id: f942fa8e-3c4d-e857-e053-6394a90a4a65

Reported adverse events (FAERS/openFDA)#

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