NDC 75140-002 Kaydia Patch

Kaydia Patch

NDC Product Code 75140-002

NDC 75140-002-01

Package Description: 166 g in 1 BOX

NDC Product Information

Kaydia Patch with NDC 75140-002 is a a human over the counter drug product labeled by Strong Current Enterprises Limited. The generic name of Kaydia Patch is kaydia patch. The product's dosage form is patch and is administered via topical form.

Labeler Name: Strong Current Enterprises Limited

Dosage Form: Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Kaydia Patch Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • CAMPHOR (NATURAL) 3 g/100g
  • LEVOMENTHOL 1 g/100g
  • CANNABIDIOL .15 g/100g

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • 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)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Strong Current Enterprises Limited
Labeler Code: 75140
Marketing Category: UNAPPROVED DRUG OTHER - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 05-02-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Kaydia Patch Product Label Images

Kaydia Patch Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

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

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%

* Please review the disclaimer below.