Label: KAYDIA PATCH patch

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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.

Drug Label Information

Updated May 1, 2020

If you are a consumer or patient please visit this version.

View All Sections
  • 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

  • DO NOT USE

  • 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 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

  • KEEP OUT OF REACH OF CHILDREN

  • 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

  • INGREDIENTS AND APPEARANCE
    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)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!