82597-020 NDC - ALDICOM (HOVENIA DULCIS FRUIT, PAEONIA LACTIFLORA ROOT, REHMANNIA GLUTINOSA ROOT, ASTRAGALUS PROPINQUUS ROOT, ANGELICA SINENSIS ROOT, CNIDIUM OFFICINALE ROOT, GLYCYRRHIZA URALENSIS ROOT, GINGER, JUJUBE FRUIT, CINNAMON)

Drug Information

Product NDC: 82597-020

Proprietary Name: ALDICOM

Non Proprietary Name: Hovenia Dulcis Fruit, Paeonia Lactiflora Root, Rehmannia Glutinosa Root, Astragalus Propinquus Root, Angelica Sinensis Root, Cnidium Officinale Root, Glycyrrhiza Uralensis Root, Ginger, Jujube fruit, Cinnamon

Active Ingredient(s):
  • 100 mg/15g ANGELICA SINENSIS ROOT;
  • 100 mg/15g ASTRAGALUS PROPINQUUS ROOT;
  • 50 mg/15g CINNAMON;
  • 100 mg/15g CNIDIUM OFFICINALE ROOT;
  • 80 mg/15g GINGER;
  • 80 mg/15g GLYCYRRHIZA URALENSIS ROOT;
  • 280 mg/15g HOVENIA DULCIS FRUIT;
  • 50 mg/15g JUJUBE FRUIT;
  • 250 mg/15g PAEONIA LACTIFLORA ROOT;
  • 100 mg/15g REHMANNIA GLUTINOSA ROOT


Administration Route(s): TOPICAL

Dosage Form(s): LIQUID

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

Labeler Information

Labeler Name: Wholesum Brands Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:4/1/2022

Package Information

No. Package Code Package Description Billing Unit
182597-020-025 POUCH in 1 CARTON (82597-020-02) / 15 g in 1 POUCH (82597-020-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC82597-020The 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 NAMEALDICOMThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEHovenia Dulcis Fruit, Paeonia Lactiflora Root, Rehmannia Glutinosa Root, Astragalus Propinquus Root, Angelica Sinensis Root, Cnidium Officinale Root, Glycyrrhiza Uralensis Root, Ginger, Jujube fruit, CinnamonThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe 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 DATE4/1/2022This 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 NAMEWholesum Brands Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEANGELICA SINENSIS ROOT; ASTRAGALUS PROPINQUUS ROOT; CINNAMON; CNIDIUM OFFICINALE ROOT; GINGER; GLYCYRRHIZA URALENSIS ROOT; HOVENIA DULCIS FRUIT; JUJUBE FRUIT; PAEONIA LACTIFLORA ROOT; REHMANNIA GLUTINOSA ROOTAn 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 STRENGTH100; 100; 50; 100; 80; 80; 280; 50; 250; 100 
ACTIVE INGRED UNITmg/15g; mg/15g; mg/15g; mg/15g; mg/15g; mg/15g; mg/15g; mg/15g; mg/15g; mg/15g 
PHARM CLASSESAllergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Food Additives [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS] 

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