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  4. NDC Product Code: 63083-4016 Pneumonia Nosode 4016

NDC 63083-4016 Pneumonia Nosode 4016

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63083-4016?
  4. Pneumonia Nosode 4016 Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63083-4016
Proprietary Name:
Pneumonia Nosode 4016
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Professional Complementary Health Formulas
Labeler Code:
63083
Product Label ID:
d8e8d385-3806-44d0-a1bf-348c74652cb0
Start Marketing Date: [9]
08-15-1984
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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 product labeled by Professional Complementary Health Formulas. The product's dosage form is . 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.*

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:

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[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".