LK Herbal Patch

Manufacturer
CAI Industries Corp.
Effective date
2025-09-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:38:46

Label at a glance#

ProductLK Herbal Patch
Active ingredientLEVOMENTHOL
Label structure7 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

FOR EXTERNAL USE ONLY

ACTIVE INGREDIENTS: Menthol 5.1%, Camphor 3.0%

WARNINGS SECTION

Do not use on open wound. KEEP OUT OF REACH OF CHILDREN.

INACTIVE INGREDIENT SECTION

Chuan Wu (Radix Aconiti), Cao Wu (Radix Aconiti Feri), Di Huang (Rehmanniae), Bai Lian (Japanese Ampelopsis Root), Gui Zhi (Cassia Twig), Bai Zhi (Fragrant Angelica), Dang Gui (Angelica), Chi Shao (Radix Paeoniae Rubra), Qiang Huo (Notopterygium Root), Ku Shen (Radix Sophorae Flavescentis), Wu Yao (Radix Linderae), Gan Cao (Liquorice), Du Huo (Heracleum Hemsleyanum Michaux), Xuan Shen (Ningpo Figwort), Da Huang (Radix Et Rhizoma Rhei), Liu Zhi (Salix Babylonica), Dong Qin Oil (Mistletoe Oil).

INDICATIONS & USAGE SECTION

For adults and children over 12 years: apply to clean and dry affected area.

BACKACHE • ARTHRITIS • STRAINS • BRUISES • SPRAINS

neck, shoulder, arm, wrist, back, waist, knee, ankle

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

OTC - PURPOSE SECTION

PAIN RELIEF
GREEN HERBAL PATCH

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2722188menthol 5.1 % Medicated PatchPSN1
2722188menthol 0.051 MG/MG Medicated PatchSCD1
2722188menthol 5.1 % Medicated PatchSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85954-002-02LK Herbal Patch10 in 1 PACKAGEPATCH101
85954-002-02LK Herbal Patch1 in 1 PATCHPATCH11

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85954-00285954-002-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
LEVOMENTHOLBZ1R15MTK7ACTIB
REHMANNIA GLUTINOSA WHOLE37S3F886KQIACT

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
56489641-368a-293a-e063-6294a90adf783f48856f-aa7a-18e7-e063-6394a90a86c92026-07-10WarningsExact identifier
spl set id: 3f48856f-aa7a-18e7-e063-6394a90a86c9

Reported adverse events (FAERS/openFDA)#

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