Pneumonia Nosode Liquid
NDC 63083-4016
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
Pneumonia Nosode is a UNAPPROVED HOMEOPATHIC-approved product labeled by Professional Complementary Health Formulas. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 63083-4016 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
63083-4016
Proprietary Name:
Pneumonia Nosode 4016
Non-Proprietary Name: [1]
Pneumonia Nosode
Substance Name: [2]
Chlamydia Trachomatis; Chlamydophila Psittaci; Coccidioides Immitis Whole; Coxiella Burnetii; Coxsackievirus A21; Haemophilus Influenzae; Histoplasma Capsulatum; Human Adenovirus B Serotype 3; Human Respiratory Syncytial Virus; Influenza A Virus A/victoria/2454/2019 Ivr-207 (h1n1) Antigen (formaldehyde Inactivated); Klebsiella Pneumoniae; Mycobacterium Tuberculosis; Mycoplasma Pneumoniae; Rickettsia Rickettsii; Staphylococcus Aureus; Streptococcus Pyogenes; Streptococcus Viridans Group
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:
Clinical Specifications
Dosage Form:
Liquid
- A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler & Regulatory Data
Labeler Name: [5]
Labeler Code:
63083
Product Label ID:
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Marketing Timeline
Start Marketing Date: [9]
08-15-1984
Listing Expiration Date: [11]
12-31-2027
Exclude Flag: [12]
N
Code Structure Chart
Product Details
What is NDC 63083-4016?
The NDC code 63083-4016 is assigned by the FDA to the product Pneumonia Nosode 4016. This pharmaceutical product is labeled by Professional Complementary Health Formulas and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 63083-4016-2. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.
What are the uses of this product?
For the temporary relief of cough, congestion, chills, difficulty breathing, or feelings of discomfort or uneasiness.*
What are Active Ingredients of this product?
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.
- CHLAMYDIA TRACHOMATIS 30 [hp_X]/59mL - Type species of CHLAMYDIA causing a variety of ocular and urogenital diseases.
- CHLAMYDOPHILA PSITTACI 30 [hp_X]/59mL - A genus of CHLAMYDOPHILA infecting primarily birds. It contains eight known serovars, some of which infect more than one type of host, including humans.
- COCCIDIOIDES IMMITIS WHOLE 30 [hp_X]/59mL
- COXIELLA BURNETII 30 [hp_X]/59mL - A species of gram-negative bacteria that grows preferentially in the vacuoles of the host cell. It is the etiological agent of Q FEVER.
- COXSACKIEVIRUS A21 30 [hp_X]/59mL
- HAEMOPHILUS INFLUENZAE 30 [hp_X]/59mL - A species of HAEMOPHILUS found on the mucous membranes of humans and a variety of animals. The species is further divided into biotypes I through VIII.
- HISTOPLASMA CAPSULATUM 30 [hp_X]/59mL
- HUMAN ADENOVIRUS B SEROTYPE 3 30 [hp_X]/59mL
- HUMAN RESPIRATORY SYNCYTIAL VIRUS 30 [hp_X]/59mL
- INFLUENZA A VIRUS A/VICTORIA/2454/2019 IVR-207 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED) 30 [hp_X]/59mL
- KLEBSIELLA PNEUMONIAE 30 [hp_X]/59mL - Gram-negative, non-motile, capsulated, gas-producing rods found widely in nature and associated with urinary and respiratory infections in humans.
- MYCOBACTERIUM TUBERCULOSIS 30 [hp_X]/59mL - A species of gram-positive, aerobic bacteria that produces TUBERCULOSIS in humans, other primates, CATTLE; DOGS; and some other animals which have contact with humans. Growth tends to be in serpentine, cordlike masses in which the bacilli show a parallel orientation.
- MYCOPLASMA PNEUMONIAE 30 [hp_X]/59mL - Short filamentous organism of the genus Mycoplasma, which binds firmly to the cells of the respiratory epithelium. It is one of the etiologic agents of non-viral primary atypical pneumonia in man.
- RICKETTSIA RICKETTSII 30 [hp_X]/59mL - A species of gram-negative, aerobic bacteria that is the etiologic agent of ROCKY MOUNTAIN SPOTTED FEVER. Its cells are slightly smaller and more uniform in size than those of RICKETTSIA PROWAZEKII.
- STAPHYLOCOCCUS AUREUS 30 [hp_X]/59mL - Potentially pathogenic bacteria found in nasal membranes, skin, hair follicles, and perineum of warm-blooded animals. They may cause a wide range of infections and intoxications.
- STREPTOCOCCUS PYOGENES 30 [hp_X]/59mL - A species of gram-positive, coccoid bacteria isolated from skin lesions, blood, inflammatory exudates, and the upper respiratory tract of humans. It is a group A hemolytic Streptococcus that can cause SCARLET FEVER and RHEUMATIC FEVER.
- STREPTOCOCCUS VIRIDANS GROUP 30 [hp_X]/59mL
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- HUMAN ADENOVIRUS B SEROTYPE 3 (UNII: 740KW2J7GZ)
- HUMAN ADENOVIRUS B SEROTYPE 3 (UNII: 740KW2J7GZ) (Active Moiety)
- CHLAMYDIA TRACHOMATIS (UNII: T6NI39QU44)
- CHLAMYDIA TRACHOMATIS (UNII: T6NI39QU44) (Active Moiety)
- CHLAMYDOPHILA PSITTACI (UNII: A16IX59JOH)
- CHLAMYDOPHILA PSITTACI (UNII: A16IX59JOH) (Active Moiety)
- COCCIDIOIDES IMMITIS WHOLE (UNII: JNF66W9FFW)
- COCCIDIOIDES IMMITIS WHOLE (UNII: JNF66W9FFW) (Active Moiety)
- COXSACKIEVIRUS A21 (UNII: 4B57CWT710)
- COXSACKIEVIRUS A21 (UNII: 4B57CWT710) (Active Moiety)
- HAEMOPHILUS INFLUENZAE (UNII: K738E2MB3I)
- HAEMOPHILUS INFLUENZAE (UNII: K738E2MB3I) (Active Moiety)
- STREPTOCOCCUS VIRIDANS GROUP (UNII: NNV2379HKR)
- STREPTOCOCCUS VIRIDANS GROUP (UNII: NNV2379HKR) (Active Moiety)
- HISTOPLASMA CAPSULATUM (UNII: 6EF1RL8Z5O)
- HISTOPLASMA CAPSULATUM (UNII: 6EF1RL8Z5O) (Active Moiety)
- INFLUENZA A VIRUS A/VICTORIA/2454/2019 IVR-207 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 2J002Y0B0W)
- INFLUENZA A VIRUS A/VICTORIA/2454/2019 IVR-207 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 2J002Y0B0W) (Active Moiety)
- KLEBSIELLA PNEUMONIAE (UNII: 09PA36CT5R)
- KLEBSIELLA PNEUMONIAE (UNII: 09PA36CT5R) (Active Moiety)
- MYCOBACTERIUM TUBERCULOSIS (UNII: R0EM8D5HFD)
- MYCOBACTERIUM TUBERCULOSIS (UNII: R0EM8D5HFD) (Active Moiety)
- MYCOPLASMA PNEUMONIAE (UNII: JQE470FAD0)
- MYCOPLASMA PNEUMONIAE (UNII: JQE470FAD0) (Active Moiety)
- STREPTOCOCCUS PYOGENES (UNII: LJ2LP0YL98)
- STREPTOCOCCUS PYOGENES (UNII: LJ2LP0YL98) (Active Moiety)
- HUMAN RESPIRATORY SYNCYTIAL VIRUS (UNII: 0980L90RNP)
- HUMAN RESPIRATORY SYNCYTIAL VIRUS (UNII: 0980L90RNP) (Active Moiety)
- COXIELLA BURNETII (UNII: GRY5SDU86N)
- COXIELLA BURNETII (UNII: GRY5SDU86N) (Active Moiety)
- RICKETTSIA RICKETTSII (UNII: V6ZO3M43L5)
- RICKETTSIA RICKETTSII (UNII: V6ZO3M43L5) (Active Moiety)
- STAPHYLOCOCCUS AUREUS (UNII: O478WX4004)
- STAPHYLOCOCCUS AUREUS (UNII: O478WX4004) (Active Moiety)
Which are the Inactive Ingredients associated 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 full disclaimer at the bottom of this page.
Product & Regulatory Definitions
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.
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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".
