NDC 64471-348 Wellguard

Aconitum Napellus, Arsenicum Iodatum, Bryonia (alba), Eupatorium Perfoliatum, Gelsemium Sempervirens, Helix Tosta, Hydrogen, Influenzinum 2019-2020, Kreosotum, Phosphorus, Teucrium Scorodonia, Thuja Occidentalis, Veratrum Viride, Anas Barbariae.

NDC Product Code 64471-348

NDC CODE: 64471-348

Proprietary Name: Wellguard What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Aconitum Napellus, Arsenicum Iodatum, Bryonia (alba), Eupatorium Perfoliatum, Gelsemium Sempervirens, Helix Tosta, Hydrogen, Influenzinum 2019-2020, Kreosotum, Phosphorus, Teucrium Scorodonia, Thuja Occidentalis, Veratrum Viride, Anas Barbariae. 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.

NDC Code Structure

  • 64471 - Source Naturals, Inc.

NDC 64471-348-01

Package Description: 25 g in 1 BOTTLE, GLASS

NDC Product Information

Wellguard with NDC 64471-348 is a a human over the counter drug product labeled by Source Naturals, Inc.. The generic name of Wellguard is aconitum napellus, arsenicum iodatum, bryonia (alba), eupatorium perfoliatum, gelsemium sempervirens, helix tosta, hydrogen, influenzinum 2019-2020, kreosotum, phosphorus, teucrium scorodonia, thuja occidentalis, veratrum viride, anas barbariae.. The product's dosage form is pellet and is administered via oral form.

Labeler Name: Source Naturals, Inc.

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.

Product Type: Human Otc Drug 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.

Wellguard Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ACONITUM NAPELLUS WHOLE 30 [hp_C]/g
  • ARSENIC TRIIODIDE 30 [hp_C]/g
  • BRYONIA ALBA ROOT 30 [hp_C]/g
  • EUPATORIUM PERFOLIATUM FLOWERING TOP 30 [hp_C]/g
  • GELSEMIUM SEMPERVIRENS ROOT 30 [hp_C]/g
  • ESCARGOT SHELL, COOKED 30 [hp_C]/g
  • HYDROGEN 30 [hp_C]/g
  • INFLUENZA A VIRUS A/BRISBANE/02/2018 IVR-190 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED) 30 [hp_C]/g
  • INFLUENZA A VIRUS A/KANSAS/14/2017 X-327 (H3N2) ANTIGEN (FORMALDEHYDE INACTIVATED) 30 [hp_C]/g
  • INFLUENZA B VIRUS B/MARYLAND/15/2016 ANTIGEN (FORMALDEHYDE INACTIVATED) 30 [hp_C]/g
  • WOOD CREOSOTE 30 [hp_C]/g
  • PHOSPHORUS 30 [hp_C]/g
  • TEUCRIUM SCORODONIA FLOWERING TOP 30 [hp_C]/g
  • THUJA OCCIDENTALIS LEAFY TWIG 30 [hp_C]/g
  • VERATRUM VIRIDE ROOT 30 [hp_C]/g
  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE 200 [hp_C]/g

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
  • SUCROSE (UNII: C151H8M554)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Source Naturals, Inc.
Labeler Code: 64471
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 04-12-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 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.

Exclude Flag: N - NO 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".

* Please review the disclaimer below.

Wellguard Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Aconitum Napellus 30C, Arsenicum Iodatum 30C, Bryonia (Alba) 30C, Eupatorium Perfoliatum 30C, Gelsemium Sempervirens 30C, Helix Tosta 30C, Hydrogen 30C, Influenzinum 2019-2020 30C, Kreosotum 30C, Phosphorus 30C, Teucrium Scorodonia 30C, Thuja Occidentalis 30C, Veratrum Viride 30C, Anas Barbariae, Hepatis ET Cordis Extractum 200C.

Indications:

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

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

Warnings:

If you are pregnant, may become pregnant, or breastfeeding,consult your health care professional before using this product.Stop use and consult your physician if symptoms persist for more than 3 days or worsen. In case of overdose, get medical help or contact a Poison Control Center right away. Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if tamper-evident seal of broken or missing. Keep out of the reach of children.

Keep Out Of Reach Of Children:

Keep out of the reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions:

Adults 17 years and up: Acute: Dissolve pellets under tongue. Take 5 pellets in mounth every 4 hours up to 4 times per day. Ongoing immune care: one level capful per month in mouth under tongue. Take 20 minutes before or after food or liquid. Consult a doctor for use in children under 17 years of age.

Inactive Ingredients:

Lactose (milk) and Sucrose.

Questions:

Manufactured for:SOURCE NATURALS, INC.P.O. BOX 2118, SANTA CRUZ, CA 95062www.sourcenaturals.com

Package Label Display:

SOURCE NATURALSWellGuardWellness Immune RemedyFormulated by Dr. Theresa DaleWITH 14 HOMEOPATHIC INGREDIENTSNEW WT. 0.88 OUNCE (25 G)

* Please review the disclaimer below.