NDC 63083-4016 Pneumonia Nosode 4016

Liquid Oral - View Dosage, Usage, Ingredients, Routes, UNII

Product Information
Product Packages
What is NDC 63083-4016?
Pneumonia Nosode 4016 Uses
Active Ingredients
Active Ingredients UNII Codes
Inactive Ingredients UNII Codes

Product Information

Get all the details for National Drug Code (NDC) 63083-4016 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

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

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 Name: [5]

Professional Complementary Health Formulas

Labeler Code:

63083

Product Label ID:

d8e8d385-3806-44d0-a1bf-348c74652cb0

Marketing Category: [8]

UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Start Marketing Date: [9]

08-15-1984

Listing Expiration Date: [11]

12-31-2027

Exclude Flag: [12]

Code Navigator:

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 which is a human over the counter drug product labeled by Professional Complementary Health Formulas. The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 63083-4016-2 59 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Pneumonia Nosode 4016?

For the temporary relief of cough, congestion, chills, difficulty breathing, or feelings of discomfort or uneasiness.*

What are Pneumonia Nosode 4016 Active Ingredients?

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 Pneumonia Nosode 4016 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 Pneumonia Nosode 4016 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.

Product Footnotes

[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, 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".

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