NDC 43742-1276 Lymph/spleen Combo
Juniperus Communis,Quercus Glandium Spiritus,Myosotis Arvensis,Natrum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43742 - Deseret Biologicals, Inc.
- 43742-1276 - Lymph/spleen Combo
Product Packages
NDC Code 43742-1276-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43742-1276?
What are the uses for Lymph/spleen Combo?
What are Lymph/spleen Combo Active Ingredients?
- ADENOSINE TRIPHOSPHATE DISODIUM 12 [hp_X]/mL
- AMBER 30 [hp_X]/mL - A yellowish fossil resin, the gum of several species of coniferous trees, found in the alluvial deposits of northeastern Germany. It is used in molecular biology in the analysis of organic matter fossilized in amber.
- APIS MELLIFERA 200 [hp_C]/mL
- CASTANEA SATIVA LEAF 4 [hp_C]/mL
- CEANOTHUS AMERICANUS LEAF 6 [hp_X]/mL
- HELIANTHUS ANNUUS FLOWERING TOP 6 [hp_X]/mL
- IRON 30 [hp_X]/mL - A metallic element with atomic symbol Fe, atomic number 26, and atomic weight 55.85. It is an essential constituent of HEMOGLOBINS; CYTOCHROMES; and IRON-BINDING PROTEINS. It plays a role in cellular redox reactions and in the transport of OXYGEN.
- JUNIPERUS COMMUNIS WHOLE 3 [hp_X]/mL
- MYOSOTIS ARVENSIS 6 [hp_X]/mL
- PHYTOLACCA AMERICANA ROOT 8 [hp_X]/mL
- QUERCUS ROBUR NUT 4 [hp_X]/mL
- QUININE ARSENATE 8 [hp_X]/mL
- SODIUM CHLORIDE 6 [hp_X]/mL - A ubiquitous sodium salt that is commonly used to season food.
- SODIUM SULFATE 6 [hp_X]/mL
- SUS SCROFA LYMPH 8 [hp_X]/mL
- SUS SCROFA SPLEEN 8 [hp_X]/mL
- SUS SCROFA THYMUS 8 [hp_X]/mL
- UBIDECARENONE 12 [hp_X]/mL
Which are Lymph/spleen Combo UNII Codes?
The UNII codes for the active ingredients in this product are:
- JUNIPERUS COMMUNIS WHOLE (UNII: 464910T5N9)
- JUNIPERUS COMMUNIS WHOLE (UNII: 464910T5N9) (Active Moiety)
- QUERCUS ROBUR NUT (UNII: Q7MU1F4GLY)
- QUERCUS ROBUR NUT (UNII: Q7MU1F4GLY) (Active Moiety)
- MYOSOTIS ARVENSIS (UNII: C73BK97H5J)
- MYOSOTIS ARVENSIS (UNII: C73BK97H5J) (Active Moiety)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
- CEANOTHUS AMERICANUS LEAF (UNII: 25B1Y14T8N)
- CEANOTHUS AMERICANUS LEAF (UNII: 25B1Y14T8N) (Active Moiety)
- HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
- HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- SUS SCROFA LYMPH (UNII: 33A7VYU29L)
- SUS SCROFA LYMPH (UNII: 33A7VYU29L) (Active Moiety)
- SUS SCROFA SPLEEN (UNII: 92AMN5J79Y)
- SUS SCROFA SPLEEN (UNII: 92AMN5J79Y) (Active Moiety)
- SUS SCROFA THYMUS (UNII: 7B69B0BD62)
- SUS SCROFA THYMUS (UNII: 7B69B0BD62) (Active Moiety)
- QUININE ARSENATE (UNII: 8C15XFK30P)
- QUININE ARSENATE (UNII: 8C15XFK30P) (Active Moiety)
- ADENOSINE TRIPHOSPHATE DISODIUM (UNII: 5L51B4DR1G)
- ADENOSINE TRIPHOSPHATE (UNII: 8L70Q75FXE) (Active Moiety)
- UBIDECARENONE (UNII: EJ27X76M46)
- UBIDECARENONE (UNII: EJ27X76M46) (Active Moiety)
- IRON (UNII: E1UOL152H7)
- IRON (UNII: E1UOL152H7) (Active Moiety)
- AMBER (UNII: 70J9Z0J26P)
- AMBER (UNII: 70J9Z0J26P) (Active Moiety)
- CASTANEA SATIVA LEAF (UNII: IV3S2HH53G)
- CASTANEA SATIVA LEAF (UNII: IV3S2HH53G) (Active Moiety)
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
Which are Lymph/spleen Combo 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 Lymph/spleen Combo?
* 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".