Degong Ling
Roselle Comprehensive Probiotics
Shenzhen Deyintang Biotechnology Co., Ltd.
Human Otc Drug
NDC 82570-011Degong Ling also known as Roselle Comprehensive Probiotics is a human otc drug labeled by 'Shenzhen Deyintang Biotechnology Co., Ltd.'. National Drug Code (NDC) number for Degong Ling is 82570-011. This drug is available in dosage form of Powder. The names of the active, medicinal ingredients in Degong Ling drug includes Collagen, Soluble, Fish Skin - 35 g/100g Hibiscus Sabdariffa Calyx - 7 g/100g . The currest status of Degong Ling drug is Active.
Drug Information:
| Drug NDC: | 82570-011 |
| 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: | Degong Ling |
| 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: | Roselle Comprehensive Probiotics |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Shenzhen Deyintang Biotechnology Co., Ltd. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Powder |
| 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: | COLLAGEN, SOLUBLE, FISH SKIN - 35 g/100g
HIBISCUS SABDARIFFA CALYX - 7 g/100g
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | TOPICAL
|
| 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 DRUG OTHER |
| 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: | 22 Feb, 2022 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 07 May, 2026 |
| 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 Deyintang Biotechnology 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: | 8JC99XGU4W
584J2XT260
|
| 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. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 82570-011-01 | 3 g in 1 POUCH (82570-011-01) | 22 Feb, 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:
Health care
Product Elements:
Degong ling roselle comprehensive probiotics hibiscus sabdariffa calyx hibiscus sabdariffa calyx bifidobacterium animalis lactis lactobacillus paracasei lactobacillus acidophilus malic acid citric acid monohydrate collagen, soluble, fish skin collagen, soluble, fish skin streptococcus thermophilus lactobacillus rhamnosus bifidobacterium bifidum bifidobacterium longum cranberry sucralose silicon dioxide limosilactobacillus reuteri
Indications and Usage:
Please eat according to the recommended amount, it is not beneficial to eat too much
Warnings:
1.please avoid children taking it by themselves. 2.please eat according to the recommended amount, it is not beneficial to eat too much. 3.please keep in a cool and dry place and avoid direct sunlight and high temperature.
Dosage and Administration:
How to eat 1 sachet each time, add 150-200ml of cool white water to brew, stir well and eat.
Package Label Principal Display Panel:
Label