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NDC 50181-0073 All Flu

Aconitum Napellus,Arsenicum Iodatum,Bryonia (alba),Eupatorium Perfoliatum,Gelsemium - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50181-0073?
  4. All Flu Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

Get all the details for National Drug Code (NDC) 50181-0073 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:
50181-0073
Proprietary Name:
All Flu
Non-Proprietary Name: [1]
Aconitum Napellus, Arsenicum Iodatum, Bryonia (alba), Eupatorium Perfoliatum, Gelsemium Sempervirens, Helix Tosta, Hydrogen, Influenzinum, Kreosotum, Phosphorus, Teucrium Scorodonia, Thuja Occidentalis, Veratrum Viride, Anas Barbariae, Hepatis Et Cordis Extractum
Substance Name: [2]
Aconitum Napellus Whole; Arsenic Triiodide; Bryonia Alba Root; Cairina Moschata Heart/liver Autolysate; Escargot Shell, Cooked; Eupatorium Perfoliatum Flowering Top; Gelsemium Sempervirens Root; Hydrogen; Influenza A Virus A/brisbane/02/2018 Ivr-190 (h1n1) Antigen (formaldehyde Inactivated); Influenza A Virus A/kansas/14/2017 X-327 (h3n2) Antigen (formaldehyde Inactivated); Influenza B Virus B/maryland/15/2016 Antigen (formaldehyde Inactivated); Phosphorus; Teucrium Scorodonia Flowering Top; Thuja Occidentalis Leafy Twig; Veratrum Viride Root; Wood Creosote
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Pellet - A small sterile solid mass consisting of a highly purified drug (with or without excipients) made by the formation of granules, or by compression and molding.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler Name: [5]
The Wellness Center For Research And Education
Labeler Code:
50181
Product Label ID:
68ee7dc5-6555-4393-9e71-7cb06c627bf0
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
12-22-2020
End Marketing Date: [10]
12-03-2025
Exclude Flag: [12]
N
Code Navigator:

Code Structure Chart

Product Details

What is NDC 50181-0073?

The NDC code 50181-0073 is assigned by the FDA to the product All Flu which is a human over the counter drug product labeled by The Wellness Center For Research And Education. The generic name of All Flu is aconitum napellus, arsenicum iodatum, bryonia (alba), eupatorium perfoliatum, gelsemium sempervirens, helix tosta, hydrogen, influenzinum, kreosotum, phosphorus, teucrium scorodonia, thuja occidentalis, veratrum viride, anas barbariae, hepatis et cordis extractum. The product's dosage form is pellet and is administered via oral form. The product is distributed in a single package with assigned NDC code 50181-0073-1 25 g in 1 bottle, glass . 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 All Flu?

Fever, chills, cough, headache and may reduce the duration and severity of ALL FLU symptoms. Fever, chills, cough, headache and may reduce the duration and severity of ALL FLU symptoms.

What are All Flu 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.

Which are All Flu UNII Codes?

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

  • ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD)
  • ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
  • ARSENIC TRIIODIDE (UNII: 3029988O2T)
  • ARSENIC CATION (3+) (UNII: C96613F5AV) (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)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
  • ESCARGOT SHELL, COOKED (UNII: 0H4593GXGV)
  • ESCARGOT SHELL, COOKED (UNII: 0H4593GXGV) (Active Moiety)
  • HYDROGEN (UNII: 7YNJ3PO35Z)
  • HYDROGEN (UNII: 7YNJ3PO35Z) (Active Moiety)
  • INFLUENZA A VIRUS A/BRISBANE/02/2018 IVR-190 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: XW4JB03TI5)
  • INFLUENZA A VIRUS A/BRISBANE/02/2018 IVR-190 (H1N1) HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 92XE6GHC89) (Active Moiety)
  • INFLUENZA A VIRUS A/KANSAS/14/2017 X-327 (H3N2) ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 3NZW5ND3D6)
  • INFLUENZA A VIRUS A/KANSAS/14/2017 X-327 (H3N2) HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: K329YCD1N9) (Active Moiety)
  • INFLUENZA B VIRUS B/MARYLAND/15/2016 ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 8V4458342X)
  • INFLUENZA B VIRUS B/MARYLAND/15/2016 HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: OES3CXI7E9) (Active Moiety)
  • WOOD CREOSOTE (UNII: 3JYG22FD73)
  • WOOD CREOSOTE (UNII: 3JYG22FD73) (Active Moiety)
  • PHOSPHORUS (UNII: 27YLU75U4W)
  • PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
  • TEUCRIUM SCORODONIA FLOWERING TOP (UNII: LOK3I16O7G)
  • TEUCRIUM SCORODONIA FLOWERING TOP (UNII: LOK3I16O7G) (Active Moiety)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
  • VERATRUM VIRIDE ROOT (UNII: 197B3Q7T5Q)
  • VERATRUM VIRIDE ROOT (UNII: 197B3Q7T5Q) (Active Moiety)
  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY)
  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY) (Active Moiety)

Which are All Flu 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

[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.

[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

[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".