Gout
Gout Ointment
Shenzhen Boceda New Technology Co., Ltd.
Human Otc Drug
NDC 82877-001Gout also known as Gout Ointment is a human otc drug labeled by 'Shenzhen Boceda New Technology Co., Ltd.'. National Drug Code (NDC) number for Gout is 82877-001. This drug is available in dosage form of Ointment. The names of the active, medicinal ingredients in Gout drug includes Chlorhexidine Acetate - .03 g/100g . The currest status of Gout drug is Active.
Drug Information:
| Drug NDC: | 82877-001 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| Proprietary Name: | Gout |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. |
| Non Proprietary Name: | Gout Ointment |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Shenzhen Boceda New Technology Co., Ltd. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Ointment |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. |
| Substance Name: | CHLORHEXIDINE ACETATE - .03 g/100g
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | CUTANEOUS
|
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
Marketing Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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. |
| Marketing Start Date: | 07 Jul, 2022 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 22 Dec, 2025 |
| 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. |
| Listing Expiration Date: | 31 Dec, 2023 |
| This is the date when the listing record will expire if not updated or certified by the firm. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | Shenzhen Boceda New Technology Co., Ltd.
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UNII: | 5908ZUF22Y
|
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. |
| Pharmacologic Class: | Decreased Cell Wall Integrity [PE]
|
| These are the reported pharmacological class categories corresponding to the SubstanceNames listed above. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 82877-001-01 | 20 g in 1 BOX (82877-001-01) | 07 Jul, 2022 | N/A | No |
| 82877-001-02 | 30 g in 1 BOX (82877-001-02) | 07 Jul, 2022 | N/A | No |
| 82877-001-03 | 50 g in 1 BOX (82877-001-03) | 07 Jul, 2022 | N/A | No |
| 82877-001-04 | 100 g in 1 BOX (82877-001-04) | 07 Jul, 2022 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. |
Purpose:
Purpose skin antibacterial
Product Elements:
Gout gout ointment chlorhexidine acetate chlorhexidine water cauliflower menthol myrrh
Indications and Usage:
Use inhibitory effect on staphylococcus aureus, escherichia coli, candida albicans for external use only.
Warnings:
Warnings keep out of reach of children. if swallowed, get medical help or contact a poison control center right away
Do Not Use:
Warnings keep out of reach of children. if swallowed, get medical help or contact a poison control center right away
When Using:
When using section when using this product keep out of eyes, ears, and mouth. in case of contact with eyes, rinse eyes thoroughly with water. stop use and ask a doctor if irritation or rash occurs. these may be signs of a serious condition. keep out of reach of children. if swallowed, get medical help or contact a poison control center right away
Dosage and Administration:
Directions place enough product on hands to cover all surfaces. massage to absorb supervise children under 6 years of age when using this product to avoid swallowing.
Stop Use:
Otc - stop use section stop use and ask a doctor if iritation or rash occurs.these may be signs of a serious condition.
Package Label Principal Display Panel:
Package label - principal display panel 82877-001-01 82877-001-02 82877-001-03 82877-001-04