NDC 43857-0444 Influaforce

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
43857-0444
Proprietary Name:
Influaforce
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bioactive Nutritional, Inc.
Labeler Code:
43857
Start Marketing Date: [9]
02-28-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 43857-0444-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 43857-0444?

The NDC code 43857-0444 is assigned by the FDA to the product Influaforce which is product labeled by Bioactive Nutritional, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43857-0444-1 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 Influaforce?

For temporary relief of minor aches and pains in muscles and joints, fever with dryness of mucous membranes and dry cough; muscular soreness and fatigue with headache. For temporary relief of minor aches and pains in muscles and joints, fever with dryness of mucous membranes and dry cough; muscular soreness and fatigue with headache.

Which are Influaforce UNII Codes?

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

  • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
  • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
  • LOMATIUM DISSECTUM ROOT (UNII: 5329928G5N)
  • LOMATIUM DISSECTUM ROOT (UNII: 5329928G5N) (Active Moiety)
  • MYRRH (UNII: JC71GJ1F3L)
  • MYRRH (UNII: JC71GJ1F3L) (Active Moiety)
  • NASTURTIUM OFFICINALE (UNII: YH89GMV676)
  • NASTURTIUM OFFICINALE (UNII: YH89GMV676) (Active Moiety)
  • TABEBUIA IMPETIGINOSA BARK (UNII: 6GLA1946WX)
  • HANDROANTHUS IMPETIGINOSUS BARK (UNII: 6GLA1946WX) (Active Moiety)
  • GOLDENSEAL (UNII: ZW3Z11D0JV)
  • GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
  • PROPOLIS WAX (UNII: 6Y8XYV2NOF)
  • BEE PROPOLIS EXTRACT (UNII: 6Y8XYV2NOF) (Active Moiety)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
  • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E)
  • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (Active Moiety)
  • FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
  • FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
  • IPECAC (UNII: 62I3C8233L)
  • IPECAC (UNII: 62I3C8233L) (Active Moiety)
  • MERCURIC CHLORIDE (UNII: 53GH7MZT1R)
  • MERCURIC CATION (UNII: ED30FJ8Y42) (Active Moiety)
  • RANCID BEEF (UNII: 29SUH5R3HU)
  • RANCID BEEF (UNII: 29SUH5R3HU) (Active Moiety)
  • INFLUENZA A VIRUS A/SINGAPORE/GP1908/2015 IVR-180A (H1N1) ANTIGEN (PROPIOLACTONE INACTIVATED) (UNII: 9JWN7VDQ7N)
  • INFLUENZA A VIRUS A/SINGAPORE/GP1908/2015 IVR-180A (H1N1) HEMAGGLUTININ ANTIGEN (PROPIOLACTONE INACTIVATED) (UNII: U6C4GJ6WZG) (Active Moiety)
  • INFLUENZA A VIRUS A/HONG KONG/4801/2014 X-263B (H3N2) ANTIGEN (PROPIOLACTONE INACTIVATED) (UNII: 3DZY3Q314E)
  • INFLUENZA A VIRUS A/HONG KONG/4801/2014 X-263B (H3N2) HEMAGGLUTININ ANTIGEN (PROPIOLACTONE INACTIVATED) (UNII: C2C4DA5K06) (Active Moiety)
  • INFLUENZA B VIRUS B/BRISBANE/60/2008 ANTIGEN (PROPIOLACTONE INACTIVATED) (UNII: 293LSV29OL)
  • INFLUENZA B VIRUS B/BRISBANE/60/2008 HEMAGGLUTININ ANTIGEN (PROPIOLACTONE INACTIVATED) (UNII: 45E2IPU4MG) (Active Moiety)

Which are Influaforce 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".