NDC 61626-0108 Flora Plus
Aloe,Alumina,Antimon Crud,Arg Nit,Chelidonium - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61626 - Net Remedies
- 61626-0108 - Flora Plus
Product Packages
NDC Code 61626-0108-4
Package Description: 59.1 mL in 1 BOTTLE
Product Details
What is NDC 61626-0108?
What are Flora Plus Active Ingredients?
- ALOE VERA LEAF 12 [hp_X]/59.1mL
- ALUMINUM OXIDE 12 [hp_X]/59.1mL - An oxide of aluminum, occurring in nature as various minerals such as bauxite, corundum, etc. It is used as an adsorbent, desiccating agent, and catalyst, and in the manufacture of dental cements and refractories.
- ANTIMONY TRISULFIDE 12 [hp_X]/59.1mL
- CHELIDONIUM MAJUS 12 [hp_X]/59.1mL - A plant species of the family PAPAVERACEAE. The common name greater celandine is similar to lesser celandine (Ficaria verna), and celandine poppy (Stylophorum diphyllum). It has been used in folk medicine and its latex contains biologically active compounds including BENZOPHENANTHRIDINES alkaloids (e.g., Chelerythrine).
- GAMBOGE 12 [hp_X]/59.1mL - A plant genus of the family CLUSIACEAE. Members contain XANTHONES.
- GOLDENSEAL 12 [hp_X]/59.1mL
- GRAPHITE 12 [hp_X]/59.1mL - An allotropic form of carbon that is used in pencils, as a lubricant, and in matches and explosives. It is obtained by mining and its dust can cause lung irritation.
- LYCOPODIUM CLAVATUM SPORE 12 [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.
- SILVER NITRATE 12 [hp_X]/59.1mL - A silver salt with powerful germicidal activity. It has been used topically to prevent OPHTHALMIA NEONATORUM.
Which are Flora Plus UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALOE VERA LEAF (UNII: ZY81Z83H0X) (Active Moiety)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ALUMINUM OXIDE (UNII: LMI26O6933) (Active Moiety)
- ANTIMONY TRISULFIDE (UNII: F79059A38U)
- ANTIMONY TRISULFIDE (UNII: F79059A38U) (Active Moiety)
- SILVER NITRATE (UNII: 95IT3W8JZE)
- SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- GAMBOGE (UNII: 7556HJ7587)
- GAMBOGE (UNII: 7556HJ7587) (Active Moiety)
- GRAPHITE (UNII: 4QQN74LH4O)
- GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
Which are Flora Plus 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WATER (UNII: 059QF0KO0R)
* 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".