FDA.reportPublic FDA data

Kaydia Patch

Manufacturer
STRONG CURRENT ENTERPRISES LIMITED
Effective date
2020-05-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:11:15

Label at a glance#

ProductKaydia Patch
Active ingredientCAMPHOR (NATURAL), LEVOMENTHOL, CANNABIDIOL
Label structure8 sections

Dosage and administration

1.Remove backing film 2.Apply patch on dry and clean skin 3.Remove and discard patch after 8-10 hours

Storage and handling

​Store in dry, cool place Avoid direct sunlight exposure Seal bag after opening to keep product fresh

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

CBD 0.15%, Camphor 3%, Mentholum 1%, Capsicum Annuum Extract 0.12%

Warning

WARNINGS SECTION

For external use only, do not ingest
Do not use on wounds,rash or damaged skin
Do not use if you have skin allergy
Not suitable for expectant mothers

when using this product

OTC - WHEN USING SECTION

Use only as directed
Apply on clean and dry skin only
Avoid area near eye, mouth or other mucous opening
Do not use with combination with a heating device
Do not apply more than 1 large patch at a time

OTC - STOP USE SECTION

Stop using this product and consult a doctor if:Condition worsens
Allergic reaction like rash, itching and other skin irritation developed
Keep out of reach of children
If ingested, seek medical/poison control attention immediately

Directions

DOSAGE & ADMINISTRATION SECTION

1.Remove backing film
2.Apply patch on dry and clean skin
3.Remove and discard patch after 8-10 hours

Other information

STORAGE AND HANDLING SECTION

​Store in dry, cool place
Avoid direct sunlight exposure
Seal bag after opening to keep product fresh

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water 56.53%, glycerin 25%, ammonium polyacrylate 9%, alcohol 3%, sodium acrylate 1.5%, 2,4-Imidazolidinedione 0.2%, disodium edta 0.1%, tartaric acid 0.25%, aluminum glycinate 0.15%

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

166 g label166 g label

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CANNABIDIOL Pharmacologic Class Indexing1Indexing - Pharmacologic Class20210608

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
4d7a96d5-8256-4268-9a6c-25ea66d321feProduct name120180814

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75140-002-012022-01-28C16284748780-1d6a99b39-f29d-a426-e053-dadaa90af4c2Kaydia Patch

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75140-002-01Kaydia Patch166 g in 1 BOXPATCH1661

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75140-002KAYDIA PATCH PATCH [STRONG CURRENT ENTERPRISES LIMITED]1Legacy NDC, 1 package rows20200514_a52fb379-a3a4-fe09-e053-2a95a90a1284.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
75140-00275140-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAMPHOR (NATURAL)N20HL7Q941ACTIB
LEVOMENTHOLBZ1R15MTK7ACTIB
WATER059QF0KO0RIACT
TARTARIC ACIDW4888I119HIACT
DIHYDROXYALUMINUM AMINOACETATEDO250MG0W6IACT
ALCOHOL3K9958V90MIACT
HYDANTOINI6208298TAIACT
CANNABIDIOL19GBJ60SN5ACTIB
GLYCERINPDC6A3C0OXIACT
SODIUM ACRYLATE7C98FKB43HIACT
DISODIUM EDTA-COPPER CU-644J875U5U11IACT

Source Document#

Source XML · Source PDF

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
a4a162ad-0652-4e05-e053-2a95a90aad10a52fb379-a3a4-fe09-e053-2a95a90a12842020-05-01WarningsExact identifier
spl id: a4a162ad-0652-4e05-e053-2a95a90aad10
spl set id: a52fb379-a3a4-fe09-e053-2a95a90a1284

Reported adverse events (FAERS/openFDA)#

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