NDC 61626-0107 Para Solve
Calc Carb,Chenopodium Anth,Cina,Croton,Filix Mas,Gambocia,Granatum,Lycopodium,Merc - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61626 - Net Remedies
- 61626-0107 - Para Solve
Product Packages
NDC Code 61626-0107-4
Package Description: 59 mL in 1 BOTTLE
Product Details
What is NDC 61626-0107?
What are Para Solve Active Ingredients?
- ARTEMISIA CINA PRE-FLOWERING TOP 12 [hp_X]/59.1mL
- CROTON TIGLIUM SEED 12 [hp_X]/59.1mL
- DRYOPTERIS FILIX-MAS ROOT 12 [hp_X]/59.1mL
- DYSPHANIA AMBROSIOIDES 12 [hp_X]/59.1mL
- GAMBOGE 12 [hp_X]/59.1mL - A plant genus of the family CLUSIACEAE. Members contain XANTHONES.
- GINGER 12 [hp_X]/59.1mL
- LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/59.1mL
- MERCURIC CHLORIDE 12 [hp_X]/59.1mL - Mercury chloride (HgCl2). A highly toxic compound that volatizes slightly at ordinary temperature and appreciably at 100 degrees C. It is corrosive to mucous membranes and used as a topical antiseptic and disinfectant.
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/59.1mL
- PUNICA GRANATUM ROOT BARK 12 [hp_X]/59.1mL
- SANTONIN 12 [hp_X]/59.1mL - Anthelmintic isolated from the dried unexpanded flower heads of Artemisia maritima and other species of Artemisia found principally in Russian and Chinese Turkestan and the Southern Ural region. (From Merck, 11th ed.)
- SENNA LEAF 12 [hp_X]/59.1mL
- SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 12 [hp_X]/59.1mL
- SPIGELIA ANTHELMIA 12 [hp_X]/59.1mL
- TANACETUM VULGARE TOP 12 [hp_X]/59.1mL
- TEUCRIUM MARUM 12 [hp_X]/59.1mL
- TIN 12 [hp_X]/59.1mL - A trace element that is required in bone formation. It has the atomic symbol Sn, atomic number 50, and atomic weight 118.71.
Which are Para Solve UNII Codes?
The UNII codes for the active ingredients in this product are:
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- DYSPHANIA AMBROSIOIDES (UNII: 4H5RSU087I)
- CHENOPODIUM AMBROSIOIDES (UNII: 4H5RSU087I) (Active Moiety)
- ARTEMISIA CINA PRE-FLOWERING TOP (UNII: 28M1820ACT)
- ARTEMISIA CINA FLOWER (UNII: 28M1820ACT) (Active Moiety)
- CROTON TIGLIUM SEED (UNII: 0HK2GZK66E)
- CROTON TIGLIUM SEED (UNII: 0HK2GZK66E) (Active Moiety)
- DRYOPTERIS FILIX-MAS ROOT (UNII: C0ZK0RRF5X)
- DRYOPTERIS FILIX-MAS ROOT (UNII: C0ZK0RRF5X) (Active Moiety)
- GAMBOGE (UNII: 7556HJ7587)
- GAMBOGE (UNII: 7556HJ7587) (Active Moiety)
- PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D)
- PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- MERCURIC CHLORIDE (UNII: 53GH7MZT1R)
- MERCURIC CATION (UNII: ED30FJ8Y42) (Active Moiety)
- SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- SANTONIN (UNII: 1VL8J38ERO)
- SANTONIN (UNII: 1VL8J38ERO) (Active Moiety)
- SENNA LEAF (UNII: AK7JF626KX)
- SENNA LEAF (UNII: AK7JF626KX) (Active Moiety)
- SPIGELIA ANTHELMIA (UNII: WYT05213GE)
- SPIGELIA ANTHELMIA (UNII: WYT05213GE) (Active Moiety)
- TIN (UNII: 387GMG9FH5)
- TIN (UNII: 387GMG9FH5) (Active Moiety)
- TANACETUM VULGARE TOP (UNII: D52957JQ8M)
- TANACETUM VULGARE TOP (UNII: D52957JQ8M) (Active Moiety)
- TEUCRIUM MARUM (UNII: 10464S0TAA)
- TEUCRIUM MARUM (UNII: 10464S0TAA) (Active Moiety)
- GINGER (UNII: C5529G5JPQ)
- GINGER (UNII: C5529G5JPQ) (Active Moiety)
Which are Para Solve 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)
Which are the Pharmacologic Classes for Para Solve?
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Food Additives - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant 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".