KAYDIA PATCH- kaydia patch patch 
STRONG CURRENT ENTERPRISES LIMITED

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Kaydia Patch


Active Ingredients

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

​Purpose

​Uses


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

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

KAYDIA PATCH 
kaydia patch patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75140-002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)3 g  in 100 g
LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7) LEVOMENTHOL1 g  in 100 g
CANNABIDIOL (UNII: 19GBJ60SN5) (CANNABIDIOL - UNII:19GBJ60SN5) CANNABIDIOL0.15 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
TARTARIC ACID (UNII: W4888I119H)  
DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)  
ALCOHOL (UNII: 3K9958V90M)  
HYDANTOIN (UNII: I6208298TA)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM ACRYLATE (UNII: 7C98FKB43H)  
DISODIUM EDTA-COPPER CU-64 (UNII: 4J875U5U11)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:75140-002-01166 g in 1 BOX; Type 0: Not a Combination Product05/02/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/02/2020
Labeler - STRONG CURRENT ENTERPRISES LIMITED (685811978)
Registrant - STRONG CURRENT ENTERPRISES LIMITED (685811978)
Establishment
NameAddressID/FEIBusiness Operations
STRONG CURRENT ENTERPRISES LIMITED685811978manufacture(75140-002)

Revised: 5/2020
Document Id: a4a162ad-0652-4e05-e053-2a95a90aad10
Set id: a52fb379-a3a4-fe09-e053-2a95a90a1284
Version: 1
Effective Time: 20200501
 
STRONG CURRENT ENTERPRISES LIMITED