NDC 64578-0142 Drainage-tone
Calcarea Iodata,Capsicum Annuum,Coenzyme A,Echinacea Angustifolia,Equisetum - View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 64578-0142?
What are the uses for Drainage-tone?
What are Drainage-tone Active Ingredients?
- CALCIUM IODIDE 12 [hp_X]/59.1mL
- CAPSICUM 6 [hp_X]/59.1mL - A plant genus of the family SOLANACEAE. The hot peppers yield CAPSAICIN, which activates VANILLOID RECEPTORS. Several varieties have sweet or pungent edible fruits that are used as vegetables when fresh and spices when the pods are dried.
- COD LIVER OIL 15 [hp_X]/59.1mL - Oil obtained from fresh livers of the cod family, Gadidae. It is a source of VITAMIN A and VITAMIN D.
- COENZYME A 8 [hp_X]/59.1mL
- ECHINACEA ANGUSTIFOLIA 4 [hp_X]/59.1mL - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
- EQUISETUM ARVENSE TOP 6 [hp_X]/59.1mL
- GOLDENSEAL 5 [hp_X]/59.1mL
- NADIDE 8 [hp_X]/59.1mL
- NITRIC ACID 12 [hp_X]/59.1mL - Nitric acid (HNO3). A colorless liquid that is used in the manufacture of inorganic and organic nitrates and nitro compounds for fertilizers, dye intermediates, explosives, and many different organic chemicals. Continued exposure to vapor may cause chronic bronchitis; chemical pneumonitis may occur. (From Merck Index, 11th ed)
- PETROSELINUM CRISPUM 4 [hp_X]/59.1mL - A plant genus of the family APIACEAE used for flavoring food.
- PHYTOLACCA AMERICANA ROOT 4 [hp_X]/59.1mL
- SCROPHULARIA NODOSA 4 [hp_X]/59.1mL
- SILICON DIOXIDE 12 [hp_X]/59.1mL - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
- THUJA OCCIDENTALIS LEAFY TWIG 4 [hp_X]/59.1mL
- WHITE MUSTARD SEED 4 [hp_X]/59.1mL
Which are Drainage-tone UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM IODIDE (UNII: 8EKI9QEE2H)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- CAPSICUM (UNII: 00UK7646FG)
- CAPSICUM (UNII: 00UK7646FG) (Active Moiety)
- COENZYME A (UNII: SAA04E81UX)
- COENZYME A (UNII: SAA04E81UX) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z)
- EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- NADIDE (UNII: 0U46U6E8UK)
- NADIDE (UNII: 0U46U6E8UK) (Active Moiety)
- NITRIC ACID (UNII: 411VRN1TV4)
- NITRIC ACID (UNII: 411VRN1TV4) (Active Moiety)
- COD LIVER OIL (UNII: BBL281NWFG)
- COD LIVER OIL (UNII: BBL281NWFG) (Active Moiety)
- PETROSELINUM CRISPUM (UNII: 1WZA4Y92EX)
- PETROSELINUM CRISPUM (UNII: 1WZA4Y92EX) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- SCROPHULARIA NODOSA (UNII: 7H443NUB2T)
- SCROPHULARIA NODOSA (UNII: 7H443NUB2T) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- WHITE MUSTARD SEED (UNII: 25VR943RPP)
- WHITE MUSTARD SEED (UNII: 25VR943RPP) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
Which are Drainage-tone 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)
- GLYCERIN (UNII: PDC6A3C0OX)
Which are the Pharmacologic Classes for Drainage-tone?
- Allergens - [CS]
- Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
- Calcium - [CS]
- Cations, Divalent - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Phosphate Binder - [EPC] (Established Pharmacologic Class)
- Phosphate Chelating Activity - [MoA] (Mechanism of Action)
- Plant Proteins - [CS]
- Vegetable 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".