NDC 82597-020 Aldicom
Hovenia Dulcis Fruit,Paeonia Lactiflora Root,Rehmannia Glutinosa Root,Astragalus - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 82597 - Wholesum Brands Co., Ltd.
- 82597-020 - Aldicom
Product Packages
NDC Code 82597-020-02
Package Description: 5 POUCH in 1 CARTON / 15 g in 1 POUCH (82597-020-01)
Product Details
What is NDC 82597-020?
What are the uses for Aldicom?
What are Aldicom Active Ingredients?
- ANGELICA SINENSIS ROOT 100 mg/15g
- ASTRAGALUS PROPINQUUS ROOT 100 mg/15g
- CINNAMON 50 mg/15g
- CNIDIUM OFFICINALE ROOT 100 mg/15g
- GINGER 80 mg/15g
- GLYCYRRHIZA URALENSIS ROOT 80 mg/15g
- HOVENIA DULCIS FRUIT 280 mg/15g
- JUJUBE FRUIT 50 mg/15g
- PAEONIA LACTIFLORA ROOT 250 mg/15g
- REHMANNIA GLUTINOSA ROOT 100 mg/15g
Which are Aldicom UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOVENIA DULCIS FRUIT (UNII: 18F22L82RE)
- HOVENIA DULCIS FRUIT (UNII: 18F22L82RE) (Active Moiety)
- PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)
- PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P) (Active Moiety)
- REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ)
- REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ) (Active Moiety)
- ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF)
- ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF) (Active Moiety)
- ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
- ANGELICA SINENSIS ROOT (UNII: B66F4574UG) (Active Moiety)
- CNIDIUM OFFICINALE ROOT (UNII: 8S3OZD358J)
- CNIDIUM OFFICINALE ROOT (UNII: 8S3OZD358J) (Active Moiety)
- GLYCYRRHIZA URALENSIS ROOT (UNII: 42B5YD8F0K)
- GLYCYRRHIZA URALENSIS ROOT (UNII: 42B5YD8F0K) (Active Moiety)
- GINGER (UNII: C5529G5JPQ)
- GINGER (UNII: C5529G5JPQ) (Active Moiety)
- JUJUBE FRUIT (UNII: G55HNL2C70)
- JUJUBE FRUIT (UNII: G55HNL2C70) (Active Moiety)
- CINNAMON (UNII: 5S29HWU6QB)
- CINNAMON (UNII: 5S29HWU6QB) (Active Moiety)
Which are Aldicom 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:
- WATER (UNII: 059QF0KO0R)
- HONEY (UNII: Y9H1V576FH)
Which are the Pharmacologic Classes for Aldicom?
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Food Additives - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
* Please review the disclaimer below.
[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.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[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".