NDC 43742-1849 Hpyl Plus
Angelica Archangelica,Geranium Maculatum,Hydrastis Canadensis,Sinapis Nigra,Symphytum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43742 - Deseret Biologicals, Inc.
- 43742-1849 - Hpyl Plus
Product Packages
NDC Code 43742-1849-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43742-1849?
What are the uses for Hpyl Plus?
What are Hpyl Plus Active Ingredients?
- ACETIC ACID 9 [hp_X]/mL - Product of the oxidation of ethanol and of the destructive distillation of wood. It is used locally, occasionally internally, as a counterirritant and also as a reagent. (Stedman, 26th ed)
- ANGELICA ARCHANGELICA ROOT 6 [hp_X]/mL
- BISMUTH SUBNITRATE 12 [hp_X]/mL
- BLACK MUSTARD SEED 6 [hp_X]/mL
- COMFREY ROOT 6 [hp_X]/mL
- DAPHNE MEZEREUM BARK 12 [hp_X]/mL
- EUPHORBIA RESINIFERA RESIN 12 [hp_X]/mL
- GERANIUM MACULATUM ROOT 6 [hp_X]/mL
- GOLDENSEAL 6 [hp_X]/mL
- GRAPHITE 12 [hp_X]/mL - An allotropic form of carbon that is used in pencils, as a lubricant, and in matches and explosives. It is obtained by mining and its dust can cause lung irritation.
- IRIS VERSICOLOR ROOT 12 [hp_X]/mL
- KRAMERIA LAPPACEA ROOT 6 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
- MARSDENIA CONDURANGO BARK 12 [hp_X]/mL
- ORNITHOGALUM UMBELLATUM 10 [hp_X]/mL
- PHENOL 9 [hp_X]/mL - An antiseptic and disinfectant aromatic alcohol.
- SEMECARPUS ANACARDIUM JUICE 12 [hp_X]/mL
- STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
- TSUGA CANADENSIS WHOLE 10 [hp_X]/mL
- URANYL NITRATE HEXAHYDRATE 12 [hp_X]/mL
Which are Hpyl Plus UNII Codes?
The UNII codes for the active ingredients in this product are:
- ANGELICA ARCHANGELICA ROOT (UNII: DTN01M69SN)
- ANGELICA ARCHANGELICA ROOT (UNII: DTN01M69SN) (Active Moiety)
- GERANIUM MACULATUM ROOT (UNII: 93IXI5B6OJ)
- GERANIUM MACULATUM ROOT (UNII: 93IXI5B6OJ) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- BLACK MUSTARD SEED (UNII: 8LTY55LQ8D)
- BLACK MUSTARD SEED (UNII: 8LTY55LQ8D) (Active Moiety)
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
- KRAMERIA LAPPACEA ROOT (UNII: P29ZH1A35Z)
- KRAMERIA LAPPACEA ROOT (UNII: P29ZH1A35Z) (Active Moiety)
- ACETIC ACID (UNII: Q40Q9N063P)
- ACETIC ACID (UNII: Q40Q9N063P) (Active Moiety)
- PHENOL (UNII: 339NCG44TV)
- PHENOL (UNII: 339NCG44TV) (Active Moiety)
- ORNITHOGALUM UMBELLATUM (UNII: 9NS3M2Y78S)
- ORNITHOGALUM UMBELLATUM (UNII: 9NS3M2Y78S) (Active Moiety)
- TSUGA CANADENSIS WHOLE (UNII: 4E0768623E)
- TSUGA CANADENSIS WHOLE (UNII: 4E0768623E) (Active Moiety)
- SEMECARPUS ANACARDIUM JUICE (UNII: Y0F0BU8RDU)
- SEMECARPUS ANACARDIUM JUICE (UNII: Y0F0BU8RDU) (Active Moiety)
- BISMUTH SUBNITRATE (UNII: H19J064BA5)
- BISMUTH CATION (UNII: ZS9CD1I8YE) (Active Moiety)
- MARSDENIA CONDURANGO BARK (UNII: R23QIR6YBA)
- MARSDENIA CONDURANGO BARK (UNII: R23QIR6YBA) (Active Moiety)
- GRAPHITE (UNII: 4QQN74LH4O)
- GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
- IRIS VERSICOLOR ROOT (UNII: X43D4L3DQC)
- IRIS VERSICOLOR ROOT (UNII: X43D4L3DQC) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV) (Active Moiety)
- URANYL NITRATE HEXAHYDRATE (UNII: 3V057702FY)
- URANIUM CATION (6+) (UNII: 5PI36AS4G7) (Active Moiety)
- EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K)
- EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
Which are Hpyl Plus 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 Hpyl Plus?
- Allergens - [CS]
- Bismuth - [CS]
- Bismuth - [EPC] (Established Pharmacologic Class)
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- 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.
[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
[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".