NDC 66096-115 Cough Relief
Aconitum Nap,Antimon Crud,Antimon Sulph,Antimon Tart,Aralia Rac,Bryonia,Chelidonium - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 66096 - Ohm Pharma Inc.
- 66096-115 - Cough Relief
Product Packages
NDC Code 66096-115-05
Package Description: 59 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 66096-115?
What are the uses for Cough Relief?
What are Cough Relief Active Ingredients?
- ACONITUM NAPELLUS 6 [hp_X]/59mL - A plant genus of the family RANUNCULACEAE. Members contain a number of diterpenoid alkaloids including: aconitans, hypaconitine, ACONITINE, jesaconitine, ignavine, napelline, and mesaconitine. The common name of Wolfbane is similar to the common name for ARNICA.
- ANTIMONY PENTASULFIDE 8 [hp_X]/59mL
- ANTIMONY POTASSIUM TARTRATE 8 [hp_X]/59mL - A schistosomicide possibly useful against other parasites. It has irritant emetic properties and may cause lethal cardiac toxicity among other adverse effects.
- ANTIMONY TRISULFIDE 8 [hp_X]/59mL
- ARALIA RACEMOSA ROOT 4 [hp_X]/59mL
- BRYONIA ALBA ROOT 6 [hp_X]/59mL
- CALCIUM SULFIDE 12 [hp_X]/59mL
- CHELIDONIUM MAJUS 6 [hp_X]/59mL - A plant species of the family PAPAVERACEAE. The common name greater celandine is similar to lesser celandine (Ficaria verna), and celandine poppy (Stylophorum diphyllum). It has been used in folk medicine and its latex contains biologically active compounds including BENZOPHENANTHRIDINES alkaloids (e.g., Chelerythrine).
- COPPER 12 [hp_X]/59mL - A heavy metal trace element with the atomic symbol Cu, atomic number 29, and atomic weight 63.55.
- DROSERA ROTUNDIFOLIA 6 [hp_X]/59mL
- POTASSIUM CARBONATE 12 [hp_X]/59mL
- SPONGIA OFFICINALIS SKELETON, ROASTED 6 [hp_X]/59mL
Which are Cough Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACONITUM NAPELLUS (UNII: U0NQ8555JD)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
- ANTIMONY TRISULFIDE (UNII: F79059A38U)
- ANTIMONY TRISULFIDE (UNII: F79059A38U) (Active Moiety)
- ANTIMONY PENTASULFIDE (UNII: 1433F1I86N)
- ANTIMONY PENTASULFIDE (UNII: 1433F1I86N) (Active Moiety)
- ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3)
- ANTIMONY CATION (3+) (UNII: 069647RPT5) (Active Moiety)
- ARALIA RACEMOSA ROOT (UNII: T90W4582DU)
- ARALIA RACEMOSA ROOT (UNII: T90W4582DU) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- COPPER (UNII: 789U1901C5)
- COPPER (UNII: 789U1901C5) (Active Moiety)
- DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ)
- DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ) (Active Moiety)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID)
- SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (Active Moiety)
Which are Cough Relief 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
Which are the Pharmacologic Classes for Cough Relief?
* 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".