NDC 63479-0409 D09 Sns-drn
Ambrosia Artemisiaefolia,Aralia Racemosa,Arnica Montana,Calendula Officinalis,Chromicum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 63479-0409?
What are the uses for D09 Sns-drn?
What are D09 Sns-drn Active Ingredients?
- AMBROSIA ARTEMISIIFOLIA 3 [hp_X]/mL
- ARALIA RACEMOSA ROOT 3 [hp_X]/mL
- ARNICA MONTANA 9 [hp_X]/mL
- CALENDULA OFFICINALIS FLOWERING TOP 2 [hp_X]/mL
- CHROMIUM TRIOXIDE 8 [hp_X]/mL
- COMFREY ROOT 8 [hp_X]/mL
- COW MILK 15 [hp_X]/mL
- ECHINACEA PURPUREA 1 [hp_X]/mL - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
- EUCALYPTOL 4 [hp_X]/mL - A monoterpene and cyclohexanol derivative that is the major component of EUCALYPTUS OIL. It is used in mouthwash, insect repellent, and as a cough suppressant, and also is widely used as a flavoring agent and solvent. It has antimicrobial properties.
- MERCURIC SULFIDE 8 [hp_X]/mL
- MERCUROUS IODIDE 8 [hp_X]/mL
- POTASSIUM CHLORIDE 8 [hp_X]/mL - A white crystal or crystalline powder used in BUFFERS; FERTILIZERS; and EXPLOSIVES. It can be used to replenish ELECTROLYTES and restore WATER-ELECTROLYTE BALANCE in treating HYPOKALEMIA.
- POTASSIUM DICHROMATE 8 [hp_X]/mL - Chromic acid (H2Cr2O7), dipotassium salt. A compound having bright orange-red crystals and used in dyeing, staining, tanning leather, as bleach, oxidizer, depolarizer for dry cells, etc. Medically it has been used externally as an astringent, antiseptic, and caustic. When taken internally, it is a corrosive poison.
- POTASSIUM SULFATE 8 [hp_X]/mL
- ROSA DAMASCENA FLOWERING TOP 3 [hp_X]/mL
- SANGUINARINE NITRATE 8 [hp_X]/mL
- SCHOENOCAULON OFFICINALE SEED 6 [hp_X]/mL
- SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE 8 [hp_X]/mL
Which are D09 Sns-drn UNII Codes?
The UNII codes for the active ingredients in this product are:
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- POTASSIUM SULFATE (UNII: 1K573LC5TV)
- MERCURIC SULFIDE (UNII: ZI0T668SF1)
- MERCURIC CATION (UNII: ED30FJ8Y42) (Active Moiety)
- SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE (UNII: 90ZQ7G407W)
- ARSENATE ION (UNII: G1DBI405OK) (Active Moiety)
- ROSA DAMASCENA FLOWERING TOP (UNII: 21W82Q764G)
- ROSA DAMASCENA FLOWERING TOP (UNII: 21W82Q764G) (Active Moiety)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- ECHINACEA PURPUREA (UNII: QI7G114Y98) (Active Moiety)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (Active Moiety)
- AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A)
- AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A) (Active Moiety)
- ARALIA RACEMOSA ROOT (UNII: T90W4582DU)
- ARALIA RACEMOSA ROOT (UNII: T90W4582DU) (Active Moiety)
- EUCALYPTOL (UNII: RV6J6604TK)
- EUCALYPTOL (UNII: RV6J6604TK) (Active Moiety)
- COW MILK (UNII: 917J3173FT)
- COW MILK (UNII: 917J3173FT) (Active Moiety)
- SANGUINARINE NITRATE (UNII: BOP122S791)
- NITRATE ION (UNII: T93E9Y2844) (Active Moiety)
- CHROMIUM TRIOXIDE (UNII: 8LV49809UC)
- CHROMIUM TRIOXIDE (UNII: 8LV49809UC) (Active Moiety)
- POTASSIUM DICHROMATE (UNII: T4423S18FM)
- DICHROMATE ION (UNII: 9LKY4BFN2V) (Active Moiety)
- MERCUROUS IODIDE (UNII: HT0935F2JR)
- MERCUROUS IODIDE (UNII: HT0935F2JR) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
Which are D09 Sns-drn 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for D09 Sns-drn?
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Milk Proteins - [CS]
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Potassium Compounds - [CS]
- Potassium Salt - [EPC] (Established Pharmacologic Class)
* 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".