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  4. NDC Product Code: 77008-4285 Chi. Joa (anti-inflammatory Effect, Antibacterial Effect, Stomatitis Improvement, Plaque Removal)

NDC 77008-4285 Chi. Joa (anti-inflammatory Effect, Antibacterial Effect, Stomatitis Improvement, Plaque Removal)

Sea Salt,Bamboo Salt,Lactobacillus Powder Powder Topical - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 77008-4285?
  4. Chi. Joa (anti-inflammatory Effect, Antibacterial Effect, Stomatitis Improvement, Plaque Removal) Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
77008-4285
Proprietary Name:
Chi. Joa (anti-inflammatory Effect, Antibacterial Effect, Stomatitis Improvement, Plaque Removal)
Non-Proprietary Name: [1]
Sea Salt, Bamboo Salt, Lactobacillus Powder
Substance Name: [2]
Cinnamon; Levomenthol; Menthol; Myrrh; Pear; Peppermint; Sea Salt; Silicon Dioxide; Sorbitol; Xylitol
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Administration Route(s): [4]
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Labeler Name: [5]
    Bioherb Co., Ltd.
    Labeler Code:
    77008
    Product Label ID:
    0042e9a0-9692-d7e0-e063-6294a90ae6c6
    Marketing Category: [8]
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date: [9]
    07-11-2023
    End Marketing Date: [10]
    07-10-2024
    Exclude Flag: [12]
    N
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    Code Structure Chart

    Product Details

    What is NDC 77008-4285?

    The NDC code 77008-4285 is assigned by the FDA to the product Chi. Joa (anti-inflammatory Effect, Antibacterial Effect, Stomatitis Improvement, Plaque Removal) which is a human over the counter drug product labeled by Bioherb Co., Ltd.. The generic name of Chi. Joa (anti-inflammatory Effect, Antibacterial Effect, Stomatitis Improvement, Plaque Removal) is sea salt, bamboo salt, lactobacillus powder. The product's dosage form is powder and is administered via topical form. The product is distributed in a single package with assigned NDC code 77008-4285-1 24 g in 1 package . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Chi. Joa (anti-inflammatory Effect, Antibacterial Effect, Stomatitis Improvement, Plaque Removal)?

    Fluids metabolism smoothBlood metabolism smoothReducing body fatElimination of waste in bloodRemove swellingAcquiring gastrointestinal satisfactionReducing food intake

    What are Chi. Joa (anti-inflammatory Effect, Antibacterial Effect, Stomatitis Improvement, Plaque Removal) Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
    • CINNAMON 1 g/100g
    • LEVOMENTHOL 1 g/100g
    • MENTHOL 1 g/100g - A monoterpene cyclohexanol produced from mint oils.
    • MYRRH 1 g/100g
    • PEAR 1 g/100g - A plant genus of the family ROSACEAE known for the edible fruit.
    • PEPPERMINT 1 g/100g
    • SEA SALT 47 g/100g
    • SILICON DIOXIDE 1 g/100g - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
    • SORBITOL 1 g/100g - A polyhydric alcohol with about half the sweetness of sucrose. Sorbitol occurs naturally and is also produced synthetically from glucose. It was formerly used as a diuretic and may still be used as a laxative and in irrigating solutions for some surgical procedures. It is also used in many manufacturing processes, as a pharmaceutical aid, and in several research applications.
    • XYLITOL 1 g/100g - A five-carbon sugar alcohol derived from XYLOSE by reduction of the carbonyl group. It is as sweet as sucrose and used as a noncariogenic sweetener.

    Which are Chi. Joa (anti-inflammatory Effect, Antibacterial Effect, Stomatitis Improvement, Plaque Removal) UNII Codes?

    The UNII codes for the active ingredients in this product are:

    Which are Chi. Joa (anti-inflammatory Effect, Antibacterial Effect, Stomatitis Improvement, Plaque Removal) Inactive Ingredients UNII Codes?

    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. The UNII codes for the inactive ingredients in this product are:

    Which are the Pharmacologic Classes for Chi. Joa (anti-inflammatory Effect, Antibacterial Effect, Stomatitis Improvement, Plaque Removal)?

    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] 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.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

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

    [8] 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.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

    [12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".