Active Ingredients
CBD 0.15%, Camphor 3%, Mentholum 1%, Capsicum Annuum Extract 0.12%
Kaydia Patch
FDA Label NDC 75140-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Strong Current Enterprises Limited for the product Kaydia Patch (NDC 75140-002). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, warning, when using this product, otc - stop use, directions, other information, inactive ingredients, package label - principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warning
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
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
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
1.Remove backing film
2.Apply patch on dry and clean skin
3.Remove and discard patch after 8-10 hours
Other Information
​Store in dry, cool place
Avoid direct sunlight exposure
Seal bag after opening to keep product fresh
Inactive Ingredients
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
166 G Label (Label)
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