NDC 61626-0106 Fire
Apil Mel,Baptisia,Baryta Carb,Hamamelis,Kali Brom,Kali - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 61626-0106?
What are Fire Active Ingredients?
- APIS MELLIFERA 12 [hp_X]/59mL
- BAPTISIA TINCTORIA ROOT 12 [hp_X]/59mL
- BARIUM CARBONATE 12 [hp_X]/59mL
- DIBASIC POTASSIUM PHOSPHATE 12 [hp_X]/59mL
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 12 [hp_X]/59mL
- KEROSENE 12 [hp_X]/59mL - A refined petroleum fraction used as a fuel as well as a solvent.
- LACHESIS MUTA VENOM 12 [hp_X]/59mL
- LILIUM LANCIFOLIUM BULB 12 [hp_X]/59mL
- PHOSPHORIC ACID 12 [hp_X]/59mL
- POTASSIUM BROMIDE 12 [hp_X]/59mL
- SPIGELIA ANTHELMIA 12 [hp_X]/59mL
- SULFUR 12 [hp_X]/59mL - An element that is a member of the chalcogen family. It has an atomic symbol S, atomic number 16, and atomic weight [32.059; 32.076]. It is found in the amino acids cysteine and methionine.
- VERATRUM VIRIDE ROOT 12 [hp_X]/59mL
Which are Fire UNII Codes?
The UNII codes for the active ingredients in this product are:
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU)
- BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (Active Moiety)
- BARIUM CARBONATE (UNII: 6P669D8HQ8)
- BARIUM CATION (UNII: V645272HLN) (Active Moiety)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
- POTASSIUM BROMIDE (UNII: OSD78555ZM)
- BROMIDE ION (UNII: 952902IX06) (Active Moiety)
- DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
- LILIUM LANCIFOLIUM BULB (UNII: 47Z05W73EZ)
- LILIUM LANCIFOLIUM BULB (UNII: 47Z05W73EZ) (Active Moiety)
- KEROSENE (UNII: 1C89KKC04E)
- KEROSENE (UNII: 1C89KKC04E) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- SPIGELIA ANTHELMIA (UNII: WYT05213GE)
- SPIGELIA ANTHELMIA (UNII: WYT05213GE) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- VERATRUM VIRIDE ROOT (UNII: 197B3Q7T5Q)
- VERATRUM VIRIDE ROOT (UNII: 197B3Q7T5Q) (Active Moiety)
Which are Fire 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WATER (UNII: 059QF0KO0R)
Which are the Pharmacologic Classes for Fire?
* 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".