NDC 43406-0686 Panacode
Syzygium,Hydrastis,Adrenalinum,Pancreatinum,Pituitarum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43406 - Natural Creations, Inc
- 43406-0686 - Panacode
Product Packages
NDC Code 43406-0686-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43406-0686?
What are the uses for Panacode?
What are Panacode Active Ingredients?
- EPINEPHRINE 9 [hp_X]/mL - The active sympathomimetic hormone from the ADRENAL MEDULLA. It stimulates both the alpha- and beta- adrenergic systems, causes systemic VASOCONSTRICTION and gastrointestinal relaxation, stimulates the HEART, and dilates BRONCHI and cerebral vessels. It is used in ASTHMA and CARDIAC FAILURE and to delay absorption of local ANESTHETICS.
- GOLDENSEAL 6 [hp_X]/mL
- INSULIN PORK 12 [hp_X]/mL
- LYCOPERDON UTRIFORME FRUITING BODY 12 [hp_X]/mL
- LYCOSA TARANTULA 12 [hp_X]/mL
- PANCRELIPASE 9 [hp_X]/mL - A preparation of hog pancreatic enzymes standardized for lipase content.
- PHOSPHORIC ACID 12 [hp_X]/mL
- PHOSPHORUS 12 [hp_X]/mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
- SOLANUM LYCOPERSICUM WHOLE 12 [hp_X]/mL
- SUS SCROFA PITUITARY GLAND, POSTERIOR 9 [hp_X]/mL
- SYZYGIUM CUMINI SEED 4 [hp_X]/mL
- TURPENTINE OIL 12 [hp_X]/mL
- URANYL NITRATE HEXAHYDRATE 12 [hp_X]/mL
Which are Panacode UNII Codes?
The UNII codes for the active ingredients in this product are:
- SYZYGIUM CUMINI SEED (UNII: 820LSF646I)
- SYZYGIUM CUMINI SEED (UNII: 820LSF646I) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- EPINEPHRINE (UNII: YKH834O4BH)
- EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
- PANCRELIPASE (UNII: FQ3DRG0N5K)
- PANCRELIPASE LIPASE (UNII: 8MYC33932O) (Active Moiety)
- SUS SCROFA PITUITARY GLAND, POSTERIOR (UNII: E8S87O660T)
- SUS SCROFA PITUITARY GLAND, POSTERIOR (UNII: E8S87O660T) (Active Moiety)
- LYCOPERDON UTRIFORME FRUITING BODY (UNII: K2A74U428F)
- LYCOPERDON UTRIFORME FRUITING BODY (UNII: K2A74U428F) (Active Moiety)
- INSULIN PORK (UNII: AVT680JB39)
- INSULIN PORK (UNII: AVT680JB39) (Active Moiety)
- SOLANUM LYCOPERSICUM WHOLE (UNII: 0243Q4990L)
- SOLANUM LYCOPERSICUM (UNII: 0243Q4990L) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- LYCOSA TARANTULA (UNII: 86M454L2TT)
- LYCOSA TARANTULA (UNII: 86M454L2TT) (Active Moiety)
- TURPENTINE OIL (UNII: C5H0QJ6V7F)
- TURPENTINE OIL (UNII: C5H0QJ6V7F) (Active Moiety)
- URANYL NITRATE HEXAHYDRATE (UNII: 3V057702FY)
- URANIUM CATION (6+) (UNII: 5PI36AS4G7) (Active Moiety)
Which are Panacode 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)
Which are the Pharmacologic Classes for Panacode?
- Adrenergic alpha-Agonists - [MoA] (Mechanism of Action)
- Adrenergic beta-Agonists - [MoA] (Mechanism of Action)
- Catecholamine - [EPC] (Established Pharmacologic Class)
- Catecholamines - [CS]
- alpha-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
- beta-Adrenergic Agonist - [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".