Kaydia Patch: Package Insert and Label Information

KAYDIA PATCH- camphor (natural), levomenthol and cannabidiol 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.

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
(click image for full-size original)

KAYDIA PATCH kaydia patch patch
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:75140-002
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CAMPHOR (NATURAL) (CAMPHOR (NATURAL)) CAMPHOR (NATURAL) 3 g in 100 g
LEVOMENTHOL (LEVOMENTHOL) LEVOMENTHOL 1 g in 100 g
CANNABIDIOL (CANNABIDIOL) CANNABIDIOL 0.15 g in 100 g
Inactive Ingredients
Ingredient Name Strength
WATER
TARTARIC ACID
DIHYDROXYALUMINUM AMINOACETATE
ALCOHOL
HYDANTOIN
GLYCERIN
SODIUM ACRYLATE
DISODIUM EDTA-COPPER CU-64
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:75140-002-01 166 g in 1 BOX None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 05/02/2020
Labeler — STRONG CURRENT ENTERPRISES LIMITED (685811978)
Registrant — STRONG CURRENT ENTERPRISES LIMITED (685811978)
Establishment
Name Address ID/FEI Operations
STRONG CURRENT ENTERPRISES LIMITED 685811978 manufacture (75140-002)

Revised: 05/2020 STRONG CURRENT ENTERPRISES LIMITED

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