NDC 73421-2968 Total Flu Cld 1
Arsenicum Alb,Baptisia,Bryonia,Causticum,Cinchona,Dulcamara,Echinacea - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73421 - White Manufacturing Inc. Dba Micro-west
- 73421-2968 - Total Flu Cld 1
Product Packages
NDC Code 73421-2968-1
Package Description: 29.6 mL in 1 BOTTLE
Product Details
What is NDC 73421-2968?
What are Total Flu Cld 1 Active Ingredients?
- ARSENIC TRIOXIDE 10 [hp_X]/29.6mL - 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.
- BAPTISIA TINCTORIA ROOT 10 [hp_X]/29.6mL
- BRYONIA ALBA ROOT 10 [hp_X]/29.6mL
- CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE 35 [hp_C]/29.6mL
- CAUSTICUM 10 [hp_X]/29.6mL
- CINCHONA BARK 10 [hp_X]/29.6mL
- ECHINACEA PURPUREA 10 [hp_X]/29.6mL - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
- EUCALYPTUS GLOBULUS LEAF 10 [hp_X]/29.6mL
- EUPATORIUM PERFOLIATUM FLOWERING TOP 10 [hp_X]/29.6mL
- GELSEMIUM SEMPERVIRENS ROOT 10 [hp_X]/29.6mL
- INFLUENZA A VIRUS 10 [hp_X]/29.6mL - The type species of the genus ALPHAINFLUENZAVIRUS that causes influenza and other diseases in humans and animals. Antigenic variation occurs frequently between strains, allowing classification into subtypes and variants. Transmission is usually by aerosol (human and most non-aquatic hosts) or waterborne (ducks). Infected birds shed the virus in their saliva, nasal secretions, and feces.
- LACHESIS MUTA VENOM 10 [hp_X]/29.6mL
- LACTIC ACID, L- 10 [hp_X]/29.6mL
- PHYTOLACCA AMERICANA ROOT 10 [hp_X]/29.6mL
- SOLANUM DULCAMARA TOP 10 [hp_X]/29.6mL
- SULFUR 10 [hp_X]/29.6mL - 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.
- TOXICODENDRON PUBESCENS LEAF 10 [hp_X]/29.6mL
- WYETHIA HELENIOIDES ROOT 10 [hp_X]/29.6mL
Which are Total Flu Cld 1 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU)
- BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- CAUSTICUM (UNII: DD5FO1WKFU)
- CAUSTICUM (UNII: DD5FO1WKFU) (Active Moiety)
- CINCHONA BARK (UNII: 292E43P4I9)
- CINCHONA BARK (UNII: 292E43P4I9) (Active Moiety)
- SOLANUM DULCAMARA TOP (UNII: KPS1B1162N)
- SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (Active Moiety)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- ECHINACEA PURPUREA (UNII: QI7G114Y98) (Active Moiety)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (Active Moiety)
- EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E)
- EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- INFLUENZA A VIRUS (UNII: R9HH0NDE2E)
- INFLUENZA A VIRUS (UNII: R9HH0NDE2E) (Active Moiety)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I) (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)
- LACTIC ACID, L- (UNII: F9S9FFU82N)
- LACTIC ACID, L- (UNII: F9S9FFU82N) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N)
- WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N) (Active Moiety)
- CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY)
- CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY) (Active Moiety)
Which are Total Flu Cld 1 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
* 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".