NDC 43742-1296 Herpes Zoster Plus
Cistus Canadensis,Clematis Erecta,Croton Tiglium,Dolichos Pruriens,Iris Versicolor,Prunus - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43742 - Deseret Biologicals, Inc.
- 43742-1296 - Herpes Zoster Plus
Product Packages
NDC Code 43742-1296-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43742-1296?
What are the uses for Herpes Zoster Plus?
What are Herpes Zoster Plus Active Ingredients?
- ARSENIC TRIOXIDE 12 [hp_X]/mL - An inorganic compound with the chemical formula As2O3 that is used for the treatment of ACUTE PROMYELOCYTIC LEUKEMIA in patients who have relapsed from, or are resistant to, conventional drug therapy.
- CLEMATIS RECTA FLOWERING TOP 6 [hp_X]/mL
- COMOCLADIA DENTATA BARK/LEAF 12 [hp_X]/mL
- CROTON TIGLIUM SEED 6 [hp_X]/mL
- DAPHNE MEZEREUM BARK 12 [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.
- HELIANTHEMUM CANADENSE 6 [hp_X]/mL
- IRIS VERSICOLOR ROOT 6 [hp_X]/mL
- KALMIA LATIFOLIA LEAF 12 [hp_X]/mL
- LACHESIS MUTA VENOM 12 [hp_X]/mL
- MUCUNA PRURIENS FRUIT TRICHOME 6 [hp_X]/mL
- POTASSIUM DICHROMATE 8 [hp_X]/mL - Chromic acid (H2Cr2O7), dipotassium salt. A compound having bright orange-red crystals and used in dyeing, staining, tanning leather, as bleach, oxidizer, depolarizer for dry cells, etc. Medically it has been used externally as an astringent, antiseptic, and caustic. When taken internally, it is a corrosive poison.
- PRUNUS SPINOSA FLOWER BUD 6 [hp_X]/mL
- RANUNCULUS BULBOSUS 6 [hp_X]/mL
- THALLIUM 12 [hp_X]/mL - A heavy, bluish white metal, atomic number 81, atomic weight [204.382; 204.385], symbol Tl.
- TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/mL
- ZINC PHOSPHIDE 8 [hp_X]/mL
Which are Herpes Zoster Plus UNII Codes?
The UNII codes for the active ingredients in this product are:
- HELIANTHEMUM CANADENSE (UNII: 46G3W789Q3)
- HELIANTHEMUM CANADENSE (UNII: 46G3W789Q3) (Active Moiety)
- CLEMATIS RECTA FLOWERING TOP (UNII: 396421SP9F)
- CLEMATIS RECTA FLOWERING TOP (UNII: 396421SP9F) (Active Moiety)
- CROTON TIGLIUM SEED (UNII: 0HK2GZK66E)
- CROTON TIGLIUM SEED (UNII: 0HK2GZK66E) (Active Moiety)
- MUCUNA PRURIENS FRUIT TRICHOME (UNII: 3E271BSI0C)
- MUCUNA PRURIENS FRUIT TRICHOME (UNII: 3E271BSI0C) (Active Moiety)
- IRIS VERSICOLOR ROOT (UNII: X43D4L3DQC)
- IRIS VERSICOLOR ROOT (UNII: X43D4L3DQC) (Active Moiety)
- PRUNUS SPINOSA FLOWER BUD (UNII: 53Y84VPS2W)
- PRUNUS SPINOSA FLOWER BUD (UNII: 53Y84VPS2W) (Active Moiety)
- RANUNCULUS BULBOSUS (UNII: AEQ8NXJ0MB)
- RANUNCULUS BULBOSUS (UNII: AEQ8NXJ0MB) (Active Moiety)
- POTASSIUM DICHROMATE (UNII: T4423S18FM)
- DICHROMATE ION (UNII: 9LKY4BFN2V) (Active Moiety)
- ZINC PHOSPHIDE (UNII: 813396S1PC)
- ZINC PHOSPHIDE (UNII: 813396S1PC) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- COMOCLADIA DENTATA BARK/LEAF (UNII: VQQ72V371Q)
- COMOCLADIA DENTATA BARK/LEAF (UNII: VQQ72V371Q) (Active Moiety)
- GRAPHITE (UNII: 4QQN74LH4O)
- GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
- KALMIA LATIFOLIA LEAF (UNII: 79N6542N18)
- KALMIA LATIFOLIA LEAF (UNII: 79N6542N18) (Active Moiety)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- THALLIUM (UNII: AD84R52XLF)
- THALLIUM (UNII: AD84R52XLF) (Active Moiety)
Which are Herpes Zoster 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)
* 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".