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  4. NDC Product Code: 42731-012 Triple Flu Defense

NDC 42731-012 Triple Flu Defense

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 42731-012?
  4. Triple Flu Defense 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:
42731-012
Proprietary Name:
Triple Flu Defense
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nenningers Naturals, Llc
Labeler Code:
42731
Product Label ID:
e2b0c8ba-05bf-4add-8391-b69db61b7933
Start Marketing Date: [9]
11-27-2012
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 42731-012?

The NDC code 42731-012 is assigned by the FDA to the product Triple Flu Defense which is product labeled by Nenningers Naturals, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 42731-012-01 30 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 Triple Flu Defense?

Uses: Relieves flu-like symptoms - fatigue, body aches, headache, sore throat, cough, fever, chills, nausea, vomiting, diarrhea.

Which are Triple Flu Defense UNII Codes?

The UNII codes for the active ingredients in this product are:

  • AILANTHUS ALTISSIMA FLOWERING TWIG (UNII: 8P29O5P7XU)
  • AILANTHUS ALTISSIMA FLOWERING TWIG (UNII: 8P29O5P7XU) (Active Moiety)
  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY)
  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY) (Active Moiety)
  • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
  • ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B) (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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
  • INFLUENZA A VIRUS A/NEW CALEDONIA/20/99 (H1N1) ANTIGEN (PROPIOLACTONE INACTIVATED) (UNII: 3NPZ4Z3B94)
  • INFLUENZA A VIRUS A/NEW CALEDONIA/20/99 (H1N1) ANTIGEN (PROPIOLACTONE INACTIVATED) (UNII: 3NPZ4Z3B94) (Active Moiety)
  • INFLUENZA B VIRUS B/HONG KONG/330/2001 ANTIGEN (PROPIOLACTONE INACTIVATED) (UNII: 23CET7LDKD)
  • INFLUENZA B VIRUS B/HONG KONG/330/2001 ANTIGEN (PROPIOLACTONE INACTIVATED) (UNII: 23CET7LDKD) (Active Moiety)
  • MERCURY (UNII: FXS1BY2PGL)
  • MERCURY (UNII: FXS1BY2PGL) (Active Moiety)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
  • LOBARIA PULMONARIA (UNII: D1YM0P5Z2T)
  • LOBARIA PULMONARIA (UNII: D1YM0P5Z2T) (Active Moiety)
  • INFLUENZA A VIRUS A/PANAMA/2007/99 (H3N2) ANTIGEN (PROPIOLACTONE INACTIVATED) (UNII: 2UES30W1DF)
  • INFLUENZA A VIRUS A/PANAMA/2007/99 (H3N2) ANTIGEN (PROPIOLACTONE INACTIVATED) (UNII: 2UES30W1DF) (Active Moiety)

Which are Triple Flu Defense 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:

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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".