NDC 59469-315 Renelix
Benzoic Acid,Nitric Acid,Apis Mellifera,Berberis Vulgaris Root Bark,Colchicum Autumnale - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59469 - Pekana Naturheilmittel Gmbh
- 59469-315 - Renelix
Product Packages
NDC Code 59469-315-10
Package Description: 1 BOTTLE, GLASS in 1 BOX / 50 mL in 1 BOTTLE, GLASS
NDC Code 59469-315-40
Package Description: 1 BOTTLE, GLASS in 1 BOX / 100 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 59469-315?
What are the uses for Renelix?
What are Renelix Active Ingredients?
- APIS MELLIFERA 4 [hp_X]/50mL
- BENZOIC ACID 4 [hp_X]/50mL - A fungistatic compound that is widely used as a food preservative. It is conjugated to GLYCINE in the liver and excreted as hippuric acid.
- BERBERIS VULGARIS ROOT BARK 3 [hp_X]/50mL
- CAPSELLA BURSA-PASTORIS TOP 510 mg/50mL
- COLCHICUM AUTUMNALE BULB 12 [hp_X]/50mL
- NITRIC ACID 6 [hp_X]/50mL - Nitric acid (HNO3). A colorless liquid that is used in the manufacture of inorganic and organic nitrates and nitro compounds for fertilizers, dye intermediates, explosives, and many different organic chemicals. Continued exposure to vapor may cause chronic bronchitis; chemical pneumonitis may occur. (From Merck Index, 11th ed)
- PROTORTONIA CACTI 631 mg/50mL
- SOLIDAGO VIRGAUREA FLOWERING TOP 2913 mg/50mL
Which are Renelix UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- BENZOIC ACID (UNII: 8SKN0B0MIM) (Active Moiety)
- NITRIC ACID (UNII: 411VRN1TV4)
- NITRIC ACID (UNII: 411VRN1TV4) (Active Moiety)
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6)
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (Active Moiety)
- PROTORTONIA CACTI (UNII: LZB7TFX1LT)
- PROTORTONIA CACTI (UNII: LZB7TFX1LT) (Active Moiety)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
- CAPSELLA BURSA-PASTORIS TOP (UNII: 7D8DU3293G)
- CAPSELLA BURSA-PASTORIS TOP (UNII: 7D8DU3293G) (Active Moiety)
Which are Renelix 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)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for Renelix?
- Allergens - [CS]
- Ammonium Ion Binding Activity - [MoA] (Mechanism of Action)
- Bee Venoms - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Nitrogen Binding Agent - [EPC] (Established Pharmacologic Class)
- Standardized Insect Venom Allergenic Extract - [EPC] (Established Pharmacologic Class)
* 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".