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  4. NDC Product Code: 64471-416 Wellness Defense

NDC 64471-416 Wellness Defense

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 64471-416?
  5. Wellness Defense Uses
  6. Active Ingredients UNII Codes
  7. 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:
64471-416
Proprietary Name:
Wellness Defense
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Source Naturals, Inc.
Labeler Code:
64471
Product Label ID:
59f79499-3224-428e-bff8-b6f58a520775
Start Marketing Date: [9]
07-23-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
10 MM
Imprint(s):
H
Score:
1

Product Packages

NDC Code 64471-416-48

Package Description: 2 BLISTER PACK in 1 CARTON / 24 TABLET in 1 BLISTER PACK

Product Details

What is NDC 64471-416?

The NDC code 64471-416 is assigned by the FDA to the product Wellness Defense 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 64471-416-48 2 blister pack in 1 carton / 24 tablet in 1 blister pack. 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 Wellness Defense?

For the temporary relief of runny nose, congestion, sore throat, headache, nausea, cough, body aches, fever and chills. Best taken at first sign of immune imbalance. For the temporary relief of runny nose, congestion, sore throat, headache, nausea, cough, body aches, fever and chills. Best taken at first sign of immune imbalance.

Which are Wellness Defense UNII Codes?

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

  • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
  • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
  • ONION (UNII: 492225Q21H)
  • ONION (UNII: 492225Q21H) (Active Moiety)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
  • SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508)
  • SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (Active Moiety)
  • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E)
  • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (Active Moiety)
  • POTASSIUM DICHROMATE (UNII: T4423S18FM)
  • DICHROMATE ION (UNII: 9LKY4BFN2V) (Active Moiety)
  • PHOSPHORUS (UNII: 27YLU75U4W)
  • PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
  • ACONITUM NAPELLUS (UNII: U0NQ8555JD)
  • ACONITUM NAPELLUS (UNII: U0NQ8555JD) (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 Wellness 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".