NDC 72945-0002 Curithys

Sodium Hyaluronate

NDC Product Code 72945-0002

NDC 72945-0002-2

Package Description: 6 PATCH in 1 POUCH > 5 mg in 1 PATCH (72945-0002-1)

NDC Product Information

Curithys with NDC 72945-0002 is a a human over the counter drug product labeled by J World. The generic name of Curithys is sodium hyaluronate. The product's dosage form is patch and is administered via topical form.

Labeler Name: J World

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.

Curithys 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.

  • HYALURONATE SODIUM 94.39 mg/100mg

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.


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: J World
Labeler Code: 72945
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: 07-21-2019 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: 12-31-2020 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.

Curithys Product Label Images

Curithys 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

Otc - Active Ingredient

Sodium hyaluronate

Inactive Ingredient


Salicylic Acid




Centella Asiatica Extract

Tranexamic acid

Camellia Japonica Flower Extract

Otc - Purpose

Micro-pyramid stimulates the skin and gives moisture and nutrition to sensitive skin.

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

Remove the protective film from the patch.Attach it vertically to the desired site.Re-press on thea ttached patch every few minutes..Remove the patch after attaching for more than 1 hour.


Use it for your own use only.For external use only.Discontinue use if adverse reaction occurs.Contact a physician if symptoms persist.Store at room temperature.Do not reuse it as a disposable product.Please use it immediately after opening.

Dosage & Administration

For topical use only

* Please review the disclaimer below.