Schusslers Immune

Echinacea, Ferrum Phosphoricum, Kali Muriaticum, Zincum Gluconicum


Nartex Laboratorios Homeopaticos, S.a. De C.v.
Human Otc Drug
NDC 34666-406
Schusslers Immune also known as Echinacea, Ferrum Phosphoricum, Kali Muriaticum, Zincum Gluconicum is a human otc drug labeled by 'Nartex Laboratorios Homeopaticos, S.a. De C.v.'. National Drug Code (NDC) number for Schusslers Immune is 34666-406. This drug is available in dosage form of Tablet. The names of the active, medicinal ingredients in Schusslers Immune drug includes Echinacea, Unspecified - 3 [hp_X]/1 Ferrosoferric Phosphate - 6 [hp_X]/1 Potassium Chloride - 6 [hp_X]/1 Zinc Gluconate - 2 [hp_X]/1 . The currest status of Schusslers Immune drug is Active.

Drug Information:

Drug NDC: 34666-406
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name: Schusslers Immune
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type: Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name: Echinacea, Ferrum Phosphoricum, Kali Muriaticum, Zincum Gluconicum
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Nartex Laboratorios Homeopaticos, S.a. De C.v.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Tablet
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status: Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:ECHINACEA, UNSPECIFIED - 3 [hp_X]/1
FERROSOFERRIC PHOSPHATE - 6 [hp_X]/1
POTASSIUM CHLORIDE - 6 [hp_X]/1
ZINC GLUCONATE - 2 [hp_X]/1
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Marketing Category: UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date: 13 Jan, 2022
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 09 May, 2026
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.
Listing Expiration Date: 31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Manufacturer Name:Nartex Laboratorios Homeopaticos, S.A. de C.V.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:Yes
Whether or not the drug has been repackaged for distribution.
UPC:0844827001471
UPC stands for Universal Product Code.
UNII:4N9P6CC1DX
91GQH8I5F7
660YQ98I10
U6WSN5SQ1Z
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class:Copper Absorption Inhibitor [EPC]
Decreased Copper Ion Absorption [PE]
Increased Large Intestinal Motility [PE]
Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
Osmotic Activity [MoA]
Osmotic Laxative [EPC]
Potassium Compounds [CS]
Potassium Salt [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
34666-406-011 BOTTLE in 1 CARTON (34666-406-01) / 240 TABLET in 1 BOTTLE13 Jan, 2022N/ANo
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Purpose:

Purpose echinacea 3x hpus*................................immunostimulant ferrum phosphoricum 6x hpus*....................................anti-inflammatory kali muriaticum 6x hpus*........................anti-inflammatory, runny nose zincum gluconicum 2x hpus*..............................cold relief * the letters "hpus" indicate that the components in this product are officially monographed in the homeopathic pharmacopoeia of the united states. "x" is a homeopathic dilution. see www.nartexlabsusa.com for more information.

Product Elements:

Schusslers immune echinacea, ferrum phosphoricum, kali muriaticum, zincum gluconicum ferrosoferric phosphate ferrosoferric phosphate potassium chloride potassium cation lactose, unspecified form zinc gluconate zinc cation magnesium stearate starch, potato water sodium benzoate talc echinacea, unspecified echinacea, unspecified gelatin logonartex

Indications and Usage:

Uses supports immune health for the temporary relief of headaches and fevers associated with the common cold and flu. claims based on traditional homeopathic practice, not accepted medical evidence. these uses have not been evaluated by fda, and product has not been clinically tested.

Warnings:

Warnings do not use if you have an allergy or hypersensitivity to the components of the formula or have had a prior reaction to this product stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days rash develops if pregnant or breast feeding, consult a health professional before use. keep out of reach of children. in case of overdose, get medical help or contact a poison control center right away.

Do Not Use:

Warnings do not use if you have an allergy or hypersensitivity to the components of the formula or have had a prior reaction to this product stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days rash develops if pregnant or breast feeding, consult a health professional before use. keep out of reach of children. in case of overdose, get medical help or contact a poison control center right away.

Dosage and Administration:

Directions adults and children 12 years and older: take tablets every 8 hours. dissolves slowly in mouth. children under 12 years, consult a physician

Stop Use:

Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days rash develops

Package Label Principal Display Panel:

Ndc 34666-406-01 schussler's immune immune system support and common cold relief. supports immune health for the temporary relief of headaches and fevers associated with the common cold and flu claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated and not clinically tested. with zinc homeopathic 240 tablets 1 2

Further Questions:

Questions or comments? informacion@nartexlabs.com or call 1-877-248-1970 between 9am and 5pm cst. active ingredients are prepared in accordance with the homeopathic pharmacopoeia of the united states, and are therefore non-toxic and have no known side effects.


Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.