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Kaydia patch - Prescription Drug Labeling

Product NDC Code 75140-001
Drug Name

Kaydia patch

Type Generic
Active Ingredients
Ginger .5 g/100g
Arnica montana flower .5 g/100g
Magnesium chloride 2 g/100g
Curcumin 1 g/100g
Thiamine 1 g/100g
Piperine .2 g/100g
Pyridoxine 1 g/100g
Route TOPICAL
Dosage Form PATCH
Labeler Name Strong Current Enterprises Limited
Packages
Package NDC Code Description
75140-001-01 166 g in 1 box (75140-001-01)

Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients Turmeric yellow 1%, ginger root extract 0.5%, Arnica Montana flower extract 0.5%, Magnesium Chloride 2%, Vitamin B1 1%, Pyridoxine 1%, Bioperine 0.2%

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions 1.Remove backing film 2.Apply patch on dry and clean skin 3.Remove and discard patch after 8-10 hours

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Water 62%, glycerin 20%, sodium polyacrylate 7%,ammonium polyacrylate 3%, disodium edta 0.5%,phenoxyethanol 0.3%, chlorphenesin 0.3%, ethylhexylglycerin 0.3%,dihydroxyaluminium aminoacetate 0.2%,tartaric acid 0.2%.

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Use

Purpose

Information about the drug product’s indications for use.
​Purpose

Spl product data elements

Usually a list of ingredients in a drug product.
Kaydia Patch Kaydia Patch GINGER GINGER ARNICA MONTANA FLOWER ARNICA MONTANA FLOWER ETHYLHEXYLGLYCERIN MAGNESIUM CHLORIDE CHLORIDE ION CURCUMIN CURCUMIN DIHYDROXYALUMINUM AMINOACETATE THIAMINE THIAMINE ION GLYCERIN PIPERINE PIPERINE PYRIDOXINE PYRIDOXINE PHENOXYETHANOL CHLORPHENESIN TARTARIC ACID WATER SODIUM POLYACRYLATE (8000 MW) DISODIUM EDTA-COPPER CU-64

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Package Label - Principal Display Panel 166 g label

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
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

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
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

Storage and handling

Information about safe storage and handling of the drug product.
Other information Store in dry, cool place Avoid direct sunlight exposure Seal bag after opening to keep product fresh

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
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.

Disclaimer: Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API