NDC 75053-0002 Lymphocil
Phytolacca Decandra,Arsenicum Iodatum,Agraphis Nutans,Apium Graveolens,Eriodictyon - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75053 - Nucleic Products, Llc
- 75053-0002 - Lymphocil
Product Packages
NDC Code 75053-0002-1
Package Description: 118 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 75053-0002?
What are the uses for Lymphocil?
What are Lymphocil Active Ingredients?
- ACONITUM LYCOCTONUM WHOLE 9 [hp_C]/mL
- APIS MELLIFERA 30 [hp_C]/mL
- ARCTOSTAPHYLOS UVA-URSI LEAF 30 [hp_C]/mL
- ARSENIC TRIIODIDE 12 [hp_X]/mL
- CAPSICUM 30 [hp_C]/mL - A plant genus of the family SOLANACEAE. The hot peppers yield CAPSAICIN, which activates VANILLOID RECEPTORS. Several varieties have sweet or pungent edible fruits that are used as vegetables when fresh and spices when the pods are dried.
- CAUSTICUM 30 [hp_C]/mL
- CELERY SEED 3 [hp_C]/mL
- ERIGERON CANADENSIS WHOLE 6 [hp_C]/mL
- ERIODICTYON CALIFORNICUM LEAF 3 [hp_C]/mL
- EUONYMUS ATROPURPUREUS BRANCH BARK/ROOT BARK 6 [hp_C]/mL
- EUONYMUS EUROPAEUS SEED 9 [hp_C]/mL
- GARLIC 6 [hp_C]/mL - A species of Allium used as a spice (SPICES) and traditional remedy. It contains alliin lyase and alliin, which is converted by alliin lyase to allicin, the pungent ingredient responsible for the aroma of fresh cut garlic.
- HYACINTHOIDES NON-SCRIPTA WHOLE 12 [hp_X]/mL
- MERCURIC SULFIDE 9 [hp_C]/mL
- PHYTOLACCA AMERICANA ROOT 4 [hp_X]/mL
- SANGUINARIA CANADENSIS ROOT 30 [hp_C]/mL
- WORMWOOD 30 [hp_C]/mL
Which are Lymphocil UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- ARSENIC TRIIODIDE (UNII: 3029988O2T)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- HYACINTHOIDES NON-SCRIPTA WHOLE (UNII: 5F658PFU56)
- HYACINTHOIDES NON-SCRIPTA WHOLE (UNII: 5F658PFU56) (Active Moiety)
- CELERY SEED (UNII: 1G1EAA320L)
- CELERY SEED (UNII: 1G1EAA320L) (Active Moiety)
- ERIODICTYON CALIFORNICUM LEAF (UNII: 2Y7TIQ135H)
- ERIODICTYON CALIFORNICUM LEAF (UNII: 2Y7TIQ135H) (Active Moiety)
- GARLIC (UNII: V1V998DC17)
- GARLIC (UNII: V1V998DC17) (Active Moiety)
- ERIGERON CANADENSIS WHOLE (UNII: 16D08B0B9N)
- ERIGERON CANADENSIS (UNII: 16D08B0B9N) (Active Moiety)
- EUONYMUS ATROPURPUREUS BRANCH BARK/ROOT BARK (UNII: WJK59V19EW)
- EUONYMUS ATROPURPUREUS BRANCH BARK/ROOT BARK (UNII: WJK59V19EW) (Active Moiety)
- ACONITUM LYCOCTONUM WHOLE (UNII: EX75Q30TX6)
- ACONITUM LYCOCTONUM WHOLE (UNII: EX75Q30TX6) (Active Moiety)
- MERCURIC SULFIDE (UNII: ZI0T668SF1)
- MERCURIC CATION (UNII: ED30FJ8Y42) (Active Moiety)
- EUONYMUS EUROPAEUS SEED (UNII: XCD2B9880O)
- EUONYMUS EUROPAEUS SEED (UNII: XCD2B9880O) (Active Moiety)
- WORMWOOD (UNII: F84709P2XV)
- WORMWOOD (UNII: F84709P2XV) (Active Moiety)
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- CAUSTICUM (UNII: DD5FO1WKFU)
- CAUSTICUM (UNII: DD5FO1WKFU) (Active Moiety)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (Active Moiety)
- ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36)
- ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36) (Active Moiety)
- CAPSICUM (UNII: 00UK7646FG)
- CAPSICUM (UNII: 00UK7646FG) (Active Moiety)
Which are Lymphocil 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 Lymphocil?
- Allergens - [CS]
- Allergens - [CS]
- Bee Venoms - [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]
- Standardized Insect Venom Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Vegetable 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".