NDC 43742-1420 Healing Support
Betula (pendula) Cortex, Caltha Palustris, Galium Aparine, Thuja Occidentalis, Urtica ...

Product Information

What is NDC 43742-1420?

The NDC code 43742-1420 is assigned by the FDA to the product Healing Support which is a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Healing Support is betula (pendula) cortex, caltha palustris, galium aparine, thuja occidentalis, urtica urens, clematis erecta, hedera helix, juniperus communis, quillaja saponaria, sempervivum tectorum, echinacea (angustifolia), argentum metallicum, calcarea fluorica, nitricum acidum, sedum acre, phosphorus, apis mellifica, pyrogenium, ononis spinosa. The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 43742-1420-1 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, RxNorm crosswalk and the complete product label.

NDC Product Code43742-1420
Proprietary Name 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.		Healing Support
Non-Proprietary Name 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.		Betula (pendula) Cortex, Caltha Palustris, Galium Aparine, Thuja Occidentalis, Urtica Urens, Clematis Erecta, Hedera Helix, Juniperus Communis, Quillaja Saponaria, Sempervivum Tectorum, Echinacea (angustifolia), Argentum Metallicum, Calcarea Fluorica, Nitricum Acidum, Sedum Acre, Phosphorus, Apis Mellifica, Pyrogenium, Ononis Spinosa
Substance Name 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.		Apis Mellifera; Betula Pendula Bark; Calcium Fluoride; Caltha Palustris; Clematis Recta Flowering Top; Echinacea Angustifolia; Galium Aparine; Garlic; Hedera Helix Flowering Twig; Juniper Berry; Nitric Acid; Ononis Spinosa Whole; Phosphorus; Rancid Beef; Sedum Acre; Sempervivum Tectorum Leaf; Silver; Thuja Occidentalis Leafy Twig; Urtica Urens
Product Type 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.		Human Otc Drug
NDC Directory StatusACTIVE PRODUCT and included in NDC Directory
Dosage FormLiquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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.		Deseret Biologicals, Inc.
Labeler Code43742
Marketing Category 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.		UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.		01-10-2019
End Marketing Date 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.		08-20-2025
Exclude Flag 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". 		N
NDC Code Structure

What are the uses for Healing Support?


Product Packages

NDC Code 43742-1420-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

Product Details

What are Healing Support 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.

Healing Support Active Ingredients UNII Codes

Healing Support 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.

Pharmacologic Class(es)

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

* Please review the disclaimer below.

Healing Support Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



Active Ingredients:



Betula (Pendula) Cortex 1X, Caltha Palustris 3X, Galium Aparine 3X, Thuja Occidentalis 3X, Urtica Urens 3X, Clematis Erecta 4X, Hedera Helix 4X, Juniperus Communis 4X, Sempervivum Tectorum 4X, Echinacea (Angustifolia) 5X, Allium Sativum 6X, Argentum Metallicum 8X, Calcarea Fluorica 8X, Nitricum Acidum 8X, Sedum Acre 8X, Phosphorus 9X, Apis Mellifica 12X, Pyrogenium 12X, Ononis Spinosa 5C.


Homeopathic Indications:



For temporary relief of symptoms related to muscle and joint pain, fever, chills, nose and sinus congestion, irritated throat, and gastrointestinal discomfort.**

**These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For temporary relief of symptoms related to muscle and joint pain, fever, chills, nose and sinus congestion, irritated throat, and gastrointestinal discomfort.**

**These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.


Warnings:



Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.

If pregnant or breast-feeding, ask a health professional before use.

Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.


Keep Out Of Reach Of Children:



Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.


Directions:



1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.


Inactive Ingredients:



Demineralized Water, 25% Ethanol


Questions:



Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070 www.desbio.com


Package Label Display:



DESBIO

NDC 43742-1420-1

HOMEOPATHIC

HEALING

SUPPORT

1 FL OZ (30 ml)


* Please review the disclaimer below.