Ear Ringing

Arnica Montana, Calcarea Carbonica, Chenopodium Anthelminticum, Chininum Salicylicum, Cimicifuga Racemosa, Coffea Tosta, Kali Iodatum, Kalmia Latifolia, Magnesia Carbonica, Manganum Aceticum, Manganum Carbonicum, Mercurius Vivus, Natrum Salicylicum, Salicylicum Acidum, Thiosinaminum, Thyroidinum.

King Bio Inc.
Human Otc Drug
NDC 57955-5276

Ear Ringing also known as Arnica Montana, Calcarea Carbonica, Chenopodium Anthelminticum, Chininum Salicylicum, Cimicifuga Racemosa, Coffea Tosta, Kali Iodatum, Kalmia Latifolia, Magnesia Carbonica, Manganum Aceticum, Manganum Carbonicum, Mercurius Vivus, Natrum Salicylicum, Salicylicum Acidum, Thiosinaminum, Thyroidinum. is a human otc drug labeled by 'King Bio Inc.'. National Drug Code (NDC) number for Ear Ringing is 57955-5276. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Ear Ringing drug includes Allylthiourea - 10 [hp_X]/59mL Arnica Montana Whole - 10 [hp_X]/59mL Black Cohosh - 10 [hp_X]/59mL Coffea Arabica Seed, Roasted - 10 [hp_X]/59mL Dysphania Ambrosioides Whole - 10 [hp_X]/59mL Kalmia Latifolia Leaf - 10 [hp_X]/59mL Magnesium Carbonate - 10 [hp_X]/59mL Manganese Acetate Tetrahydrate - 10 [hp_X]/59mL Manganese Carbonate - 10 [hp_X]/59mL Mercury - 10 [hp_X]/59mL and more. The currest status of Ear Ringing drug is Active.

Drug Information:

Drug NDC:	57955-5276
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:	Ear Ringing
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:	Arnica Montana, Calcarea Carbonica, Chenopodium Anthelminticum, Chininum Salicylicum, Cimicifuga Racemosa, Coffea Tosta, Kali Iodatum, Kalmia Latifolia, Magnesia Carbonica, Manganum Aceticum, Manganum Carbonicum, Mercurius Vivus, Natrum Salicylicum, Salicylicum Acidum, Thiosinaminum, Thyroidinum.
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:	ALLYLTHIOUREA - 10 [hp_X]/59mL ARNICA MONTANA WHOLE - 10 [hp_X]/59mL BLACK COHOSH - 10 [hp_X]/59mL COFFEA ARABICA SEED, ROASTED - 10 [hp_X]/59mL DYSPHANIA AMBROSIOIDES WHOLE - 10 [hp_X]/59mL KALMIA LATIFOLIA LEAF - 10 [hp_X]/59mL MAGNESIUM CARBONATE - 10 [hp_X]/59mL MANGANESE ACETATE TETRAHYDRATE - 10 [hp_X]/59mL MANGANESE CARBONATE - 10 [hp_X]/59mL MERCURY - 10 [hp_X]/59mL Load more... OYSTER SHELL CALCIUM CARBONATE, CRUDE - 10 [hp_X]/59mL POTASSIUM IODIDE - 10 [hp_X]/59mL QUININE SALICYLATE - 10 [hp_X]/59mL SALICYLIC ACID - 10 [hp_X]/59mL SODIUM SALICYLATE - 10 [hp_X]/59mL THYROID, UNSPECIFIED - 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:	05 Dec, 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:	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.
UNII:	706IDJ14B7 O80TY208ZW K73E24S6X9 9H58JRT35E 4H5RSU087I 79N6542N18 0E53J927NA 9TO51D176N 9ZV57512ZM FXS1BY2PGL Load more... 2E32821G6I 1C4QK22F9J 6DY04L71DR O414PZ4LPZ WIQ1H85SYP 0B4FDL9I6P
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:	Magnetic Resonance Contrast Activity [MoA] Paramagnetic Contrast Agent [EPC]
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
57955-5276-2	1 BOTTLE, SPRAY in 1 CARTON (57955-5276-2) / 59 mL in 1 BOTTLE, SPRAY	05 Dec, 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

Ear Ringing

Arnica Montana & more..

Liquid
King Bio Inc.
NDC: 57955-5276

Purpose:

Equal volumes of each hpus** ingredient in 10x, 30x, and 1lm potencies. arnica montana .......................................................dull hearing calcarea carbonica ............................................ cracking in ears chenopodium anthelminticum.......................auditory nerve issues chininum salicylicum..................................................ear ringing cimicifuga racemosa............................................noise sensitivity coffea tosta .............................................ringing, roaring in ears kali iodatum..................................................................ear pain kalmia latifolia .......................................................stiches in ear magnesia carbonica ........................................diminished hearing manganum aceticum ....................................................whistling manganum carbonicum...................................................earache mercurius vivus .......................................tinkling, buzzing sounds natrum salicylicum ................................................noises in ears salicylicum acidum........................................................deafness thiosinaminum ...................................................vertigo, tinnitus thyroidinum...........................................................ear disorders **âhpusâ indicates the active ingredients are in the official homeopathic pharmacopeia of the united states. reference image:ear ringing.jpg

Product Elements:

Ear ringing arnica montana, calcarea carbonica, chenopodium anthelminticum, chininum salicylicum, cimicifuga racemosa, coffea tosta, kali iodatum, kalmia latifolia, magnesia carbonica, manganum aceticum, manganum carbonicum, mercurius vivus, natrum salicylicum, salicylicum acidum, thiosinaminum, thyroidinum. arnica montana whole arnica montana oyster shell calcium carbonate, crude oyster shell calcium carbonate, crude dysphania ambrosioides whole chenopodium ambrosioides quinine salicylate salicylic acid black cohosh black cohosh coffea arabica seed, roasted coffea arabica seed, roasted potassium iodide iodide ion kalmia latifolia leaf kalmia latifolia leaf magnesium carbonate carbonate ion manganese acetate tetrahydrate manganous cation manganese carbonate manganous cation mercury mercury sodium salicylate salicylic acid salicylic acid salicylic acid allylthiourea allylthiourea thyroid, unspecified thyroid, unspecified 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 uses for symptomatic relief of ear sounds: buzzing roaring ringing whistling sensitivity to noise â 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:ear ringing.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:ear ringing.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:ear ringing.jpg

Package Label Principal Display Panel:

Image description ear ringing.jpg

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.