NDC 68089-004 Clear Sinus And Ear
Pulsatilla Vulgaris,Euphorbia Resinifera Resin,Calcium Sulfate And Oyster Shell Calcium - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68089 - Clear Products, Inc.
- 68089-004 - Clear Sinus And Ear
Product Characteristics
Product Packages
NDC Code 68089-004-01
Package Description: 60 CAPSULE in 1 BOTTLE
Product Details
What is NDC 68089-004?
What are the uses for Clear Sinus And Ear?
What are Clear Sinus And Ear Active Ingredients?
- CALCIUM SULFATE 3 [hp_X]/1 - A calcium salt that is used for a variety of purposes including: building materials, as a desiccant, in dentistry as an impression material, cast, or die, and in medicine for immobilizing casts and as a tablet excipient. It exists in various forms and states of hydration. Plaster of Paris is a mixture of powdered and heat-treated gypsum.
- EUPHORBIA RESINIFERA RESIN 6 [hp_X]/1
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 3 [hp_X]/1
- PULSATILLA VULGARIS 3 [hp_X]/1
Which are Clear Sinus And Ear UNII Codes?
The UNII codes for the active ingredients in this product are:
- PULSATILLA VULGARIS (UNII: I76KB35JEV)
- PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
- EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K)
- EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K) (Active Moiety)
- CALCIUM SULFATE (UNII: WAT0DDB505)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
Which are Clear Sinus And Ear 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:
- PUERARIA MONTANA VAR. LOBATA ROOT (UNII: PET93F4I3C)
- ANGELICA ATROPURPUREA ROOT (UNII: 885452N0GZ)
- PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)
- PLATYCODON GRANDIFLORUS ROOT (UNII: 2DF0NS0O2Z)
- COIX LACRYMA-JOBI SEED (UNII: 4Q4V6NTZ1F)
- GINGER (UNII: C5529G5JPQ)
- PERILLA FRUTESCENS TOP (UNII: T4L5881Y68)
- SAPOSHNIKOVIA DIVARICATA ROOT (UNII: 8H84LFK2QD)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- CINNAMON (UNII: 5S29HWU6QB)
- LICORICE (UNII: 61ZBX54883)
Which are the Pharmacologic Classes for Clear Sinus And Ear?
* 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".