82570-010 NDC - DEKANGLING (PHELLINUS AND BRAZIL MUSHROOM ANTRODIA CINNAMOMEA EXTRACT POWDER)

Drug Information

Product NDC: 82570-010

Proprietary Name: Dekangling

Non Proprietary Name: Phellinus and Brazil Mushroom Antrodia cinnamomea Extract Powder

Active Ingredient(s):
  • 20 g/100g COLLAGEN, SOLUBLE, FISH SKIN;
  • 10 g/100g CORDYCEPS MILITARIS FRUITING BODY;
  • 7 g/100g CULTIVATED MUSHROOM;
  • 7 g/100g MORINGA OLEIFERA LEAF;
  • 7 g/100g POMIFERIN;
  • 4 g/100g TAIWANOFUNGUS CAMPHORATUS MYCELIUM


Administration Route(s): TOPICAL

Dosage Form(s): POWDER

Pharmacy Class(es):
  • Allergens [CS];
  • Cell-mediated Immunity [PE];
  • Dietary Proteins [CS];
  • Fungal Proteins [CS];
  • Increased Histamine Release [PE];
  • Non-Standardized Food Allergenic Extract [EPC]

Labeler Information

Labeler Name: Shenzhen Deyintang Biotechnology Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:2/21/2022

Package Information

No. Package Code Package Description Billing Unit
182570-010-013 g in 1 POUCH (82570-010-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC82570-010The 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.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMEDekanglingThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEPhellinus and Brazil Mushroom Antrodia cinnamomea Extract PowderThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEPOWDERThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE2/21/2022This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct 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.
LABELER NAMEShenzhen Deyintang Biotechnology Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMECOLLAGEN, SOLUBLE, FISH SKIN; CORDYCEPS MILITARIS FRUITING BODY; CULTIVATED MUSHROOM; MORINGA OLEIFERA LEAF; POMIFERIN; TAIWANOFUNGUS CAMPHORATUS MYCELIUMAn 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.
ACTIVE NUMERATOR STRENGTH20; 10; 7; 7; 7; 4 
ACTIVE INGRED UNITg/100g; g/100g; g/100g; g/100g; g/100g; g/100g 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Fungal Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC] 

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This page was last updated on: 2/1/2023