NDC 57955-3004 Advanced Arnica Plus
Arnica Montana,Arnica Montana,Radix,Bellis Perennis,Bryonia,Hypericum Perforatum,Lithium - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57955 - King Bio Inc.
- 57955-3004 - Advanced Arnica Plus
Product Packages
NDC Code 57955-3004-2
Package Description: 59 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 57955-3004?
What are the uses for Advanced Arnica Plus?
What are Advanced Arnica Plus Active Ingredients?
- ARNICA MONTANA ROOT 10 [hp_X]/59mL
- ARNICA MONTANA WHOLE 10 [hp_X]/59mL
- BELLIS PERENNIS WHOLE 10 [hp_X]/59mL
- BRYONIA ALBA ROOT 10 [hp_X]/59mL
- HYPERICUM PERFORATUM WHOLE 10 [hp_X]/59mL
- LITHIUM CARBONATE 10 [hp_X]/59mL - A lithium salt, classified as a mood-stabilizing agent. Lithium ion alters the metabolism of BIOGENIC MONOAMINES in the CENTRAL NERVOUS SYSTEM, and affects multiple neurotransmission systems.
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 10 [hp_X]/59mL
- PHYTOLACCA AMERICANA ROOT 10 [hp_X]/59mL
- RUTA GRAVEOLENS FLOWERING TOP 10 [hp_X]/59mL
- TOXICODENDRON PUBESCENS LEAF 10 [hp_X]/59mL
Which are Advanced Arnica Plus UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- ARNICA MONTANA ROOT (UNII: MUE8Y11327)
- ARNICA MONTANA ROOT (UNII: MUE8Y11327) (Active Moiety)
- BELLIS PERENNIS WHOLE (UNII: 2HU33I03UY)
- BELLIS PERENNIS (UNII: 2HU33I03UY) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
- LITHIUM CARBONATE (UNII: 2BMD2GNA4V)
- LITHIUM CATION (UNII: 8H8Z5UER66) (Active Moiety)
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
Which are Advanced Arnica 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:
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T)
- ORANGE PEEL (UNII: TI9T76XD44)
- CITRUS RETICULATA FRUIT OIL (UNII: 25P9H3QU5E)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- LACTIC ACID (UNII: 33X04XA5AT)
- LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
- BENZYLPENICILLOYL POLYLYSINE (UNII: 76479814OY)
- CARYA OVATA BARK (UNII: X765CF609L)
- STEVIOL (UNII: 4741LYX6RT)
Which are the Pharmacologic Classes for Advanced Arnica Plus?
- Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
- Mood Stabilizer - [EPC] (Established Pharmacologic Class)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
* 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".