Allergies And Hay Fever Reliever

Allium Cepa, Ambrosia Artemisiaefolia, Arsenicum Album, Arum Triphyllum, Arundo Mauritanica, Euphrasia Officinalis, Galphimia Glauca, Histaminum Hydrocholoricum, Kali Bichromicum, Naphthalinum, Natrum Muriaticum, Sabadilla, Solidago Virgaurea, Sticta Pulmonaria, Wyethia Helenioides.

King Bio Inc.
Human Otc Drug
NDC 57955-2805

Allergies And Hay Fever Reliever also known as Allium Cepa, Ambrosia Artemisiaefolia, Arsenicum Album, Arum Triphyllum, Arundo Mauritanica, Euphrasia Officinalis, Galphimia Glauca, Histaminum Hydrocholoricum, Kali Bichromicum, Naphthalinum, Natrum Muriaticum, Sabadilla, Solidago Virgaurea, Sticta Pulmonaria, Wyethia Helenioides. is a human otc drug labeled by 'King Bio Inc.'. National Drug Code (NDC) number for Allergies And Hay Fever Reliever is 57955-2805. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Allergies And Hay Fever Reliever drug includes Ambrosia Artemisiifolia Whole - 10 [hp_X]/59mL Arisaema Triphyllum Root - 10 [hp_X]/59mL Arsenic Trioxide - 10 [hp_X]/59mL Arundo Pliniana Root - 10 [hp_X]/59mL Euphrasia Stricta - 10 [hp_X]/59mL Galphimia Glauca Flowering Top - 10 [hp_X]/59mL Histamine Dihydrochloride - 10 [hp_X]/59mL Lobaria Pulmonaria - 10 [hp_X]/59mL Naphthalene - 10 [hp_X]/59mL Onion - 10 [hp_X]/59mL and more. The currest status of Allergies And Hay Fever Reliever drug is Active.

Drug Information:

Drug NDC:	57955-2805
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:	Allergies And Hay Fever Reliever
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:	Allium Cepa, Ambrosia Artemisiaefolia, Arsenicum Album, Arum Triphyllum, Arundo Mauritanica, Euphrasia Officinalis, Galphimia Glauca, Histaminum Hydrocholoricum, Kali Bichromicum, Naphthalinum, Natrum Muriaticum, Sabadilla, Solidago Virgaurea, Sticta Pulmonaria, Wyethia Helenioides.
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	King Bio Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Liquid
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:	AMBROSIA ARTEMISIIFOLIA WHOLE - 10 [hp_X]/59mL ARISAEMA TRIPHYLLUM ROOT - 10 [hp_X]/59mL ARSENIC TRIOXIDE - 10 [hp_X]/59mL ARUNDO PLINIANA ROOT - 10 [hp_X]/59mL EUPHRASIA STRICTA - 10 [hp_X]/59mL GALPHIMIA GLAUCA FLOWERING TOP - 10 [hp_X]/59mL HISTAMINE DIHYDROCHLORIDE - 10 [hp_X]/59mL LOBARIA PULMONARIA - 10 [hp_X]/59mL NAPHTHALENE - 10 [hp_X]/59mL ONION - 10 [hp_X]/59mL Load more... POTASSIUM DICHROMATE - 10 [hp_X]/59mL SCHOENOCAULON OFFICINALE SEED - 10 [hp_X]/59mL SODIUM CHLORIDE - 10 [hp_X]/59mL SOLIDAGO VIRGAUREA FLOWERING TOP - 10 [hp_X]/59mL WYETHIA HELENIOIDES ROOT - 10 [hp_X]/59mL
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:	31 May, 2022
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	24 Dec, 2025
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:	King Bio Inc.
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.
NUI:	N0000185371 N0000175629 N0000184306 M0000728 M0006342 M0022575
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	9W34L2CQ9A DM64K844DM S7V92P67HO ZXE7LB03WC C9642I91WL 93PH5Q8M7E 3POA0Q644U D1YM0P5Z2T 2166IN72UN 492225Q21H Load more... T4423S18FM 6NAF1689IO 451W47IQ8X 5405K23S50 J10PD1AQ0N
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 EPC:	Non-Standardized Food Allergenic Extract [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class PE:	Increased Histamine Release [PE] Cell-mediated Immunity [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:	Allergens [CS] Dietary Proteins [CS] Vegetable Proteins [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:	Allergens [CS] Cell-mediated Immunity [PE] Dietary Proteins [CS] Increased Histamine Release [PE] Non-Standardized Food Allergenic Extract [EPC] Vegetable Proteins [CS]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
57955-2805-2	1 BOTTLE, SPRAY in 1 CARTON (57955-2805-2) / 59 mL in 1 BOTTLE, SPRAY	31 May, 2022	N/A	No
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.

Other medicines with the same generic name

Allergies And Hay Fever Reliever

Allium Cepa & more..

Liquid
King Bio Inc.
NDC: 57955-2805

Purpose:

Equal volumes of each hpus ingredient in 10x, 30x, and 1lm potencies. allium cepa............. runny nose; itchy eyes, ears, nose or throat ambrosia artemisiaefolia..................nasal and sinus congestion arsenicum album ...................................... exhaustion, hay fever arum triphyllum .......................swollen glands, nasal congestion arundo mauritanica ......................... itching and burning in nose, ears, or roof of mouth euphrasia officinalis.........................sinus irritation and pressure galphimia glauca..........................................excessive sneezing histaminum hydrochloricum .............symptoms of allergic origin kali bichromicum ............................... nasal congestion, sinusitis naphthalinum ....................................................sneezing, cough natrum muriaticum..........................................itchy, watery eyes sabadilla .......................................sore throat, hay fever, vertigo solidago virgaurea ...................inflammation, mucus congestion sticta pulmonaria...................congestion, dull headache, rhinitis wyethia helenioides ............... postnasal drip, bronchial irritation hpusâ indicates the active ingredients are in the official homeopathic pharmacopeia of the united states. reference image: allergies.jpg

Product Elements:

Allergies and hay fever reliever allium cepa, ambrosia artemisiaefolia, arsenicum album, arum triphyllum, arundo mauritanica, euphrasia officinalis, galphimia glauca, histaminum hydrocholoricum, kali bichromicum, naphthalinum, natrum muriaticum, sabadilla, solidago virgaurea, sticta pulmonaria, wyethia helenioides. onion onion ambrosia artemisiifolia whole ambrosia artemisiifolia arsenic trioxide arsenic cation (3+) arisaema triphyllum root arisaema triphyllum root arundo pliniana root arundo pliniana root euphrasia stricta euphrasia stricta galphimia glauca flowering top galphimia glauca flowering top histamine dihydrochloride histamine potassium dichromate dichromate ion naphthalene naphthalene sodium chloride chloride ion schoenocaulon officinale seed schoenocaulon officinale seed solidago virgaurea flowering top solidago virgaurea flowering top lobaria pulmonaria lobaria pulmonaria wyethia helenioides root wyethia helenioides root ascorbic acid citric acid monohydrate citrus aurantium fruit oil orange peel citrus reticulata fruit oil water glycerin lactic acid, unspecified form lonicera japonica flower benzylpenicilloyl polylysine carya ovata bark steviol

Indications and Usage:

Uses for temporary relief of allergies in general including hay fever symptoms: nasal and sinus congestion runny nose sneezing coughing watery eyes as per various homeopathic materia medicas. claims based on traditional homeopathic practice, not accepted medical evidence. these uses have not been evaluated by the fda, and product has not been clinically tested. reference image: allergies.jpg

Warnings:

Warnings stop use and consult a physician if symptoms worsen or persist for more than 7 days. if pregnant or breast-feeding , ask a healthcare professional before use. keep out of reach of children. in case of overdose, get medical help or contact a poison control center immediately. reference image: allergies.jpg

Dosage and Administration:

Directions initially, depress pump until primed. spray one dose directly into mouth. adults: 3 sprays 3 times per day. children ages 6-12: 2 sprays 3 times per day. consult a physician for use in children under 6 years of age. use additionally as needed, up to 6 times per day. reference image: allergies.jpg

Package Label Principal Display Panel:

Image description allergies.jpg

Comments/ Reviews:

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