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  4. NDC Product Code: 64471-347 Wellguard

NDC 64471-347 Wellguard

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 64471-347?
  4. Wellguard 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:
64471-347
Proprietary Name:
Wellguard
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Source Naturals, Inc.
Labeler Code:
64471
Product Label ID:
8bb6d6d4-1c33-4da6-aec7-02176d373dee
Start Marketing Date: [9]
06-12-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 64471-347?

The NDC code 64471-347 is assigned by the FDA to the product Wellguard which is product labeled by Source Naturals, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 64471-347-01 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 Wellguard?

May reduce the duration and severity of signs of immune imbalance. May reduce the duration and severity of signs of immune imbalance.

Which are Wellguard UNII Codes?

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

  • ACONITUM NAPELLUS (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/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)
  • WOOD CREOSOTE (UNII: 3JYG22FD73)
  • 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 Wellguard 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".