NDC 54532-0033 Hevert Detox Liver
Milk Thistle,Chelidonium Majus Root,And Taraxacum Officinale Liquid Oral - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54532 - Hevert Arzneimittel Gmbh & Co Kg
- 54532-0033 - Hevert Detox Liver
Product Packages
NDC Code 54532-0033-5
Package Description: 1 BOTTLE in 1 CARTON / 50 mL in 1 BOTTLE
Product Details
What is NDC 54532-0033?
What are the uses for Hevert Detox Liver?
What are Hevert Detox Liver Active Ingredients?
- CHELIDONIUM MAJUS ROOT 3 [hp_X]/50mL
- MILK THISTLE 1 [hp_X]/50mL
- TARAXACUM OFFICINALE 3 [hp_X]/50mL - A plant genus of the family Asteraceae. Members contain chicoric and chlorogenic acids and germacrane- and eudesmane-type SESQUITERPENES.
Which are Hevert Detox Liver UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- CLEMATIS RECTA FLOWERING TOP (UNII: 396421SP9F)
- CLEMATIS RECTA FLOWERING TOP (UNII: 396421SP9F) (Active Moiety)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
- MERCURIC IODIDE (UNII: R03O05RB0P)
- MERCURIC IODIDE (UNII: R03O05RB0P) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- TOXICODENDRON PUBESCENS SHOOT (UNII: 46PYZ1F82M)
- TOXICODENDRON PUBESCENS SHOOT (UNII: 46PYZ1F82M) (Active Moiety)
- SCROPHULARIA NODOSA LEAF WITH STEM (UNII: K93UPA2CNQ)
- SCROPHULARIA NODOSA LEAF WITH STEM (UNII: K93UPA2CNQ) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- MILK THISTLE (UNII: U946SH95EE)
- MILK THISTLE (UNII: U946SH95EE) (Active Moiety)
- CHELIDONIUM MAJUS ROOT (UNII: FLT36UCF0N)
- CHELIDONIUM MAJUS ROOT (UNII: FLT36UCF0N) (Active Moiety)
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
- NITRIC ACID (UNII: 411VRN1TV4)
- NITRIC ACID (UNII: 411VRN1TV4) (Active Moiety)
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
- LYTTA VESICATORIA (UNII: 3Q034RO3BT)
- LYTTA VESICATORIA (UNII: 3Q034RO3BT) (Active Moiety)
- JUNIPER BERRY (UNII: O84B5194RL)
- JUNIPER BERRY (UNII: O84B5194RL) (Active Moiety)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
- EICHHORNIA CRASSIPES WHOLE (UNII: 216V7S21BH)
- EICHHORNIA CRASSIPES WHOLE (UNII: 216V7S21BH) (Active Moiety)
- OKOUBAKA AUBREVILLEI BARK (UNII: MK2074187Z)
- OKOUBAKA AUBREVILLEI BARK (UNII: MK2074187Z) (Active Moiety)
- QUASSIA AMARA WOOD (UNII: S5249Q85HW)
- QUASSIA AMARA WOOD (UNII: S5249Q85HW) (Active Moiety)
Which are Hevert Detox Liver 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
* 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".