NDC 57955-5276 Ear Ringing
Arnica Montana,Calcarea Carbonica,Chenopodium Anthelminticum,Chininum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57955 - King Bio Inc.
- 57955-5276 - Ear Ringing
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?
What are the uses for Ear Ringing?
What are Ear Ringing Active Ingredients?
- 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 - A silver metallic element that exists as a liquid at room temperature. It has the atomic symbol Hg (from hydrargyrum, liquid silver), atomic number 80, and atomic weight 200.59. Mercury is used in many industrial applications and its salts have been employed therapeutically as purgatives, antisyphilitics, disinfectants, and astringents. It can be absorbed through the skin and mucous membranes which leads to MERCURY POISONING. Because of its toxicity, the clinical use of mercury and mercurials is diminishing.
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 10 [hp_X]/59mL
- POTASSIUM IODIDE 10 [hp_X]/59mL - An inorganic compound that is used as a source of iodine in thyrotoxic crisis and in the preparation of thyrotoxic patients for thyroidectomy. (From Dorland, 27th ed)
- QUININE SALICYLATE 10 [hp_X]/59mL
- SALICYLIC ACID 10 [hp_X]/59mL - A compound obtained from the bark of the white willow and wintergreen leaves. It has bacteriostatic, fungicidal, and keratolytic actions.
- SODIUM SALICYLATE 10 [hp_X]/59mL - A non-steroidal anti-inflammatory agent that is less effective than equal doses of ASPIRIN in relieving pain and reducing fever. However, individuals who are hypersensitive to ASPIRIN may tolerate sodium salicylate. In general, this salicylate produces the same adverse reactions as ASPIRIN, but there is less occult gastrointestinal bleeding. (From AMA Drug Evaluations Annual, 1992, p120)
- THYROID, UNSPECIFIED 10 [hp_X]/59mL
Which are Ear Ringing UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- DYSPHANIA AMBROSIOIDES WHOLE (UNII: 4H5RSU087I)
- CHENOPODIUM AMBROSIOIDES (UNII: 4H5RSU087I) (Active Moiety)
- QUININE SALICYLATE (UNII: 6DY04L71DR)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- BLACK COHOSH (UNII: K73E24S6X9)
- BLACK COHOSH (UNII: K73E24S6X9) (Active Moiety)
- COFFEA ARABICA SEED, ROASTED (UNII: 9H58JRT35E)
- COFFEA ARABICA SEED, ROASTED (UNII: 9H58JRT35E) (Active Moiety)
- POTASSIUM IODIDE (UNII: 1C4QK22F9J)
- IODIDE ION (UNII: 09G4I6V86Q) (Active Moiety)
- KALMIA LATIFOLIA LEAF (UNII: 79N6542N18)
- KALMIA LATIFOLIA LEAF (UNII: 79N6542N18) (Active Moiety)
- MAGNESIUM CARBONATE (UNII: 0E53J927NA)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- MANGANESE ACETATE TETRAHYDRATE (UNII: 9TO51D176N)
- MANGANOUS CATION (UNII: H6EP7W5457) (Active Moiety)
- MANGANESE CARBONATE (UNII: 9ZV57512ZM)
- MERCURY (UNII: FXS1BY2PGL)
- MERCURY (UNII: FXS1BY2PGL) (Active Moiety)
- SODIUM SALICYLATE (UNII: WIQ1H85SYP)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- ALLYLTHIOUREA (UNII: 706IDJ14B7)
- ALLYLTHIOUREA (UNII: 706IDJ14B7) (Active Moiety)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P) (Active Moiety)
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:
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T)
- ORANGE PEEL (UNII: TI9T76XD44)
- CITRUS RETICULATA FRUIT OIL (UNII: 25P9H3QU5E)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
- LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
- BENZYLPENICILLOYL POLYLYSINE (UNII: 76479814OY)
- CARYA OVATA BARK (UNII: X765CF609L)
- STEVIOL (UNII: 4741LYX6RT)
Which are the Pharmacologic Classes for Ear Ringing?
* Please review the disclaimer below.
[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".