NDC 43742-1571 Enviroclenz
Berberis Vulgaris,Carduus Marianus,Chelidonium Majus,Glycyrrhiza Glabra,Lappa - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 43742-1571?
What are the uses for Enviroclenz?
What are Enviroclenz Active Ingredients?
- ACETONE 9 [hp_X]/mL - A colorless liquid used as a solvent and an antiseptic. It is one of the ketone bodies produced during ketoacidosis.
- AMMONIUM CHLORIDE 9 [hp_X]/mL - An acidifying agent that has expectorant and diuretic effects. Also used in etching and batteries and as a flux in electroplating.
- ARCTIUM LAPPA ROOT 3 [hp_X]/mL
- BENZENE 9 [hp_X]/mL - Toxic, volatile, flammable liquid hydrocarbon byproduct of coal distillation. It is used as an industrial solvent in paints, varnishes, lacquer thinners, gasoline, etc. Benzene causes central nervous system damage acutely and bone marrow damage chronically and is carcinogenic. It was formerly used as parasiticide.
- BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL
- CHELIDONIUM MAJUS 3 [hp_X]/mL - A plant species of the family PAPAVERACEAE. The common name greater celandine is similar to lesser celandine (Ficaria verna), and celandine poppy (Stylophorum diphyllum). It has been used in folk medicine and its latex contains biologically active compounds including BENZOPHENANTHRIDINES alkaloids (e.g., Chelerythrine).
- CHLORINE 10 [hp_X]/mL - An element with atomic symbol Cl, atomic number 17, and atomic weight 35, and member of the halogen family.
- FRANGULA ALNUS BARK 3 [hp_X]/mL
- GERMANIUM SESQUIOXIDE 8 [hp_X]/mL
- GLYCYRRHIZA GLABRA 3 [hp_X]/mL - A genus of leguminous herbs or shrubs whose roots yield GLYCYRRHETINIC ACID and its derivative, CARBENOXOLONE.
- IRIDIUM 12 [hp_X]/mL - A metallic element with the atomic symbol Ir, atomic number 77, and atomic weight 192.22.
- LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
- METHYL ALCOHOL 9 [hp_X]/mL - A colorless, flammable liquid used in the manufacture of FORMALDEHYDE and ACETIC ACID, in chemical synthesis, antifreeze, and as a solvent. Ingestion of methanol is toxic and may cause blindness.
- MILK THISTLE 3 [hp_X]/mL
- NITRIC ACID 12 [hp_X]/mL - 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)
- PHOSPHORIC ACID 12 [hp_X]/mL
- PHYTOLACCA AMERICANA ROOT 8 [hp_X]/mL
- PROPYLENE GLYCOL 9 [hp_X]/mL - A clear, colorless, viscous organic solvent and diluent used in pharmaceutical preparations.
- SODIUM LAURYL SULFATE 9 [hp_X]/mL
- SODIUM TRIPOLYPHOSPHATE 9 [hp_X]/mL
- STILLINGIA SYLVATICA ROOT 3 [hp_X]/mL
- STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
- TARAXACUM OFFICINALE FLOWERING TOP 3 [hp_X]/mL
- TRIFOLIUM PRATENSE LEAF 3 [hp_X]/mL
- TURPENTINE OIL 9 [hp_X]/mL
Which are Enviroclenz UNII Codes?
The UNII codes for the active ingredients in this product are:
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- MILK THISTLE (UNII: U946SH95EE)
- MILK THISTLE (UNII: U946SH95EE) (Active Moiety)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) (Active Moiety)
- ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
- ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) (Active Moiety)
- FRANGULA ALNUS BARK (UNII: S2D77IH61R)
- FRANGULA ALNUS BARK (UNII: S2D77IH61R) (Active Moiety)
- STILLINGIA SYLVATICA ROOT (UNII: QBR70R4FBK)
- STILLINGIA SYLVATICA ROOT (UNII: QBR70R4FBK) (Active Moiety)
- TARAXACUM OFFICINALE FLOWERING TOP (UNII: DQS85W46HV)
- TARAXACUM OFFICINALE FLOWERING TOP (UNII: DQS85W46HV) (Active Moiety)
- TRIFOLIUM PRATENSE LEAF (UNII: 612YOZ36DG)
- TRIFOLIUM PRATENSE LEAF (UNII: 612YOZ36DG) (Active Moiety)
- GERMANIUM SESQUIOXIDE (UNII: 96WE91N25T)
- GERMANIUM SESQUIOXIDE (UNII: 96WE91N25T) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- ACETONE (UNII: 1364PS73AF)
- ACETONE (UNII: 1364PS73AF) (Active Moiety)
- AMMONIUM CHLORIDE (UNII: 01Q9PC255D)
- AMMONIUM CATION (UNII: 54S68520I4) (Active Moiety)
- BENZENE (UNII: J64922108F)
- BENZENE (UNII: J64922108F) (Active Moiety)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (Active Moiety)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- LAURYL SULFATE (UNII: DIQ16UC154) (Active Moiety)
- SODIUM TRIPOLYPHOSPHATE (UNII: 5HK03SA80J)
- TRIPOLYPHOSPHATE ION (UNII: 5798IYA5AY) (Active Moiety)
- TURPENTINE OIL (UNII: C5H0QJ6V7F)
- TURPENTINE OIL (UNII: C5H0QJ6V7F) (Active Moiety)
- METHYL ALCOHOL (UNII: Y4S76JWI15)
- METHYL ALCOHOL (UNII: Y4S76JWI15) (Active Moiety)
- CHLORINE (UNII: 4R7X1O2820)
- CHLORINE (UNII: 4R7X1O2820) (Active Moiety)
- IRIDIUM (UNII: 44448S9773)
- IRIDIUM (UNII: 44448S9773) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- NITRIC ACID (UNII: 411VRN1TV4)
- NITRIC ACID (UNII: 411VRN1TV4) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
Which are Enviroclenz 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 Enviroclenz?
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage 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".