NDC 57955-5276 Ear Ringing

Arnica Montana,Calcarea Carbonica,Chenopodium Anthelminticum,Chininum - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
57955-5276
Proprietary Name:
Ear Ringing
Non-Proprietary Name: [1]
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.
Substance Name: [2]
Allylthiourea; Arnica Montana Whole; Black Cohosh; Coffea Arabica Seed, Roasted; Dysphania Ambrosioides Whole; Kalmia Latifolia Leaf; Magnesium Carbonate; Manganese Acetate Tetrahydrate; Manganese Carbonate; Mercury; Oyster Shell Calcium Carbonate, Crude; Potassium Iodide; Quinine Salicylate; Salicylic Acid; Sodium Salicylate; Thyroid, Unspecified
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Liquid - 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): [4]
  • Oral - Administration to or by way of the mouth.
  • Labeler Name: [5]
    King Bio Inc.
    Labeler Code:
    57955
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    12-05-2022
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 57955-5276-2

    Package Description: 1 BOTTLE, SPRAY in 1 CARTON / 59 mL in 1 BOTTLE, SPRAY

    Product Details

    What is NDC 57955-5276?

    The NDC code 57955-5276 is assigned by the FDA to the product Ear Ringing which is a human over the counter drug product labeled by King Bio Inc.. The generic name of Ear Ringing is 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.. 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 57955-5276-2 1 bottle, spray in 1 carton / 59 ml in 1 bottle, spray. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Ear Ringing?

    Initially, depress pump untilprimed.Spray one dose directly intomouth.Adults: 3 sprays 3 times perday.Children ages 6-12: 2 sprays 3times per day.Consult a physician for use inchildren under 6 years of age.Use additionally as needed, upto 6 times per day.Reference image:Ear Ringing.jpg

    What are Ear Ringing 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.

    Which are Ear Ringing UNII Codes?

    The UNII codes for the active ingredients in this product are:

    Which are Ear Ringing 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. The UNII codes for the inactive ingredients in this product are:

    Which are the Pharmacologic Classes for Ear Ringing?

    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.

    Product Footnotes

    [1] 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.

    [2] 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.

    [3] 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.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

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

    [8] 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.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] 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.

    [12] 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".