NDC 64616-086 Category V
Immune System Booster Liquid Oral - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64616 - Vitality Works, Inc,
- 64616-086 - Category V
Product Packages
NDC Code 64616-086-02
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 64616-086?
What are Category V Active Ingredients?
- ANAGALLIS ARVENSIS 3 [hp_X]/mL
- ANHYDROUS CITRIC ACID 15 [hp_X]/mL - A key intermediate in metabolism. It is an acid compound found in citrus fruits. The salts of citric acid (citrates) can be used as anticoagulants due to their calcium chelating ability.
- AQUA REGIA 15 [hp_X]/mL
- ARSENIC TRIIODIDE 10 [hp_X]/mL
- CALCIUM LACTATE 50 [hp_X]/mL
- CHAMAEMELUM NOBILE 20 [hp_X]/mL - A plant genus of the family ASTERACEAE that is used in folk medicine as CHAMOMILE. Other plants with similar common names include MATRICARIA; TRIPLEUROSPERMUM and ANTHEMIS.
- COPPER 25 [hp_X]/mL - A heavy metal trace element with the atomic symbol Cu, atomic number 29, and atomic weight 63.55.
- DELPHINIUM STAPHISAGRIA SEED 5 [hp_X]/mL
- EPINEPHRINE 15 [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.
- FRAXINUS AMERICANA BARK 4 [hp_X]/mL
- HEXAPLEX TRUNCULUS HYPOBRANCHIAL GLAND JUICE 14 [hp_X]/mL
- LACTIC ACID 15 [hp_X]/mL - A normal intermediate in the fermentation (oxidation, metabolism) of sugar. The concentrated form is used internally to prevent gastrointestinal fermentation. (From Stedman, 26th ed)
- PETROSELINUM CRISPUM 20 [hp_X]/mL - A plant genus of the family APIACEAE used for flavoring food.
- PICRIC ACID 12 [hp_X]/mL
- POTASSIUM CARBONATE 8 [hp_X]/mL
- SALICYLIC ACID 12 [hp_X]/mL - A compound obtained from the bark of the white willow and wintergreen leaves. It has bacteriostatic, fungicidal, and keratolytic actions.
- SALIX NIGRA BARK 20 [hp_X]/mL
- STRYCHNOS IGNATII SEED 4 [hp_X]/mL
- URANYL NITRATE HEXAHYDRATE 17 [hp_X]/mL
Which are Category V UNII Codes?
The UNII codes for the active ingredients in this product are:
- EPINEPHRINE (UNII: YKH834O4BH)
- EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
- ANAGALLIS ARVENSIS (UNII: 46883LR90E)
- ANAGALLIS ARVENSIS (UNII: 46883LR90E) (Active Moiety)
- CHAMAEMELUM NOBILE (UNII: 7NF3GE7IWR)
- CHAMAEMELUM NOBILE (UNII: 7NF3GE7IWR) (Active Moiety)
- ARSENIC TRIIODIDE (UNII: 3029988O2T)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- CALCIUM LACTATE (UNII: 2URQ2N32W3)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) (Active Moiety)
- COPPER (UNII: 789U1901C5)
- COPPER (UNII: 789U1901C5) (Active Moiety)
- FRAXINUS AMERICANA BARK (UNII: 0B24UR1O1S)
- FRAXINUS AMERICANA BARK (UNII: 0B24UR1O1S) (Active Moiety)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (Active Moiety)
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- HEXAPLEX TRUNCULUS HYPOBRANCHIAL GLAND JUICE (UNII: IQV54TN60Y)
- HEXAPLEX TRUNCULUS HYPOBRANCHIAL GLAND JUICE (UNII: IQV54TN60Y) (Active Moiety)
- AQUA REGIA (UNII: X3TT5X989E)
- AQUA REGIA (UNII: X3TT5X989E) (Active Moiety)
- PETROSELINUM CRISPUM (UNII: 1WZA4Y92EX)
- PETROSELINUM CRISPUM (UNII: 1WZA4Y92EX) (Active Moiety)
- PICRIC ACID (UNII: A49OS0F91S)
- PICRIC ACID (UNII: A49OS0F91S) (Active Moiety)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- SALIX NIGRA BARK (UNII: QU52J3A5B3)
- SALIX NIGRA BARK (UNII: QU52J3A5B3) (Active Moiety)
- LACTIC ACID (UNII: 33X04XA5AT)
- LACTIC ACID (UNII: 33X04XA5AT) (Active Moiety)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (Active Moiety)
- URANYL NITRATE HEXAHYDRATE (UNII: 3V057702FY)
- URANIUM CATION (6+) (UNII: 5PI36AS4G7) (Active Moiety)
Which are Category V 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 Category V?
- Acidifying Activity - [MoA] (Mechanism of Action)
- Acidifying Activity - [MoA] (Mechanism of Action)
- Adrenergic alpha-Agonists - [MoA] (Mechanism of Action)
- Adrenergic beta-Agonists - [MoA] (Mechanism of Action)
- Anti-coagulant - [EPC] (Established Pharmacologic Class)
- Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
- Calcium Chelating Activity - [MoA] (Mechanism of Action)
- Calcium - [CS]
- Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
- Catecholamine - [EPC] (Established Pharmacologic Class)
- Catecholamines - [CS]
- Cations, Divalent - [CS]
- Copper - [CS]
- Copper-containing Intrauterine Device - [EPC] (Established Pharmacologic Class)
- Decreased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Decreased Embryonic Implantation - [PE] (Physiologic Effect)
- Decreased Sperm Motility - [PE] (Physiologic Effect)
- Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Inhibit Ovum Fertilization - [PE] (Physiologic Effect)
- Phosphate Binder - [EPC] (Established Pharmacologic Class)
- Phosphate Chelating Activity - [MoA] (Mechanism of Action)
- 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".