NDC 83027-0003 Sciatic Formula
Kali Iodatum,Ruta Graveolens,Ammonium Muriaticum,Belladonna,Gnaphalium - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 83027 - Nutritional Specialties, Inc.
- 83027-0003 - Sciatic Formula
Product Packages
NDC Code 83027-0003-1
Package Description: 60 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 83027-0003?
What are the uses for Sciatic Formula?
What are Sciatic Formula Active Ingredients?
- ACONITUM NAPELLUS WHOLE 8 [hp_X]/mL
- AMMONIUM CHLORIDE 4 [hp_X]/mL - An acidifying agent that has expectorant and diuretic effects. Also used in etching and batteries and as a flux in electroplating.
- ARSENIC TRIOXIDE 12 [hp_X]/mL - An inorganic compound with the chemical formula As2O3 that is used for the treatment of ACUTE PROMYELOCYTIC LEUKEMIA in patients who have relapsed from, or are resistant to, conventional drug therapy.
- ATROPA BELLADONNA 6 [hp_X]/mL - A plant species of the genus ATROPA, family SOLANACEAE that contains ATROPINE; SCOPOLAMINE; BELLADONNA ALKALOIDS and other SOLANACEOUS ALKALOIDS. Some species in this genus are called deadly nightshade which is also a common name for SOLANUM.
- CITRULLUS COLOCYNTHIS FRUIT PULP 7 [hp_X]/mL
- POTASSIUM IODIDE 3 [hp_X]/mL - 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)
- PSEUDOGNAPHALIUM OBTUSIFOLIUM WHOLE 6 [hp_X]/mL
- RUTA GRAVEOLENS FLOWERING TOP 3 [hp_X]/mL
- STRYCHNOS NUX-VOMICA SEED 8 [hp_X]/mL
Which are Sciatic Formula UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM IODIDE (UNII: 1C4QK22F9J)
- IODIDE ION (UNII: 09G4I6V86Q) (Active Moiety)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
- AMMONIUM CHLORIDE (UNII: 01Q9PC255D)
- AMMONIUM CATION (UNII: 54S68520I4) (Active Moiety)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
- PSEUDOGNAPHALIUM OBTUSIFOLIUM WHOLE (UNII: 36XQ854NWW)
- PSEUDOGNAPHALIUM OBTUSIFOLIUM (UNII: 36XQ854NWW) (Active Moiety)
- CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17)
- CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (Active Moiety)
- ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
Which are Sciatic Formula 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 Sciatic Formula?
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
* 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".