61626-0107 NDC - PARA SOLVE (CALC CARB, CHENOPODIUM ANTH, CINA, CROTON, FILIX MAS, GAMBOCIA, GRANATUM, LYCOPODIUM, MERC CORROS, NAT PHOS, SANTONINUM, SENNA, SPIGELIA ANTH, STANNUM MET, TANACETUM, TEURICUM MAR, ZINGIBER)

Drug Information

Product NDC: 61626-0107

Proprietary Name: Para Solve

Non Proprietary Name: Calc carb, Chenopodium anth, Cina, Croton, Filix Mas, Gambocia, Granatum, Lycopodium, Merc corros, Nat phos, Santoninum, Senna, Spigelia anth, Stannum met, Tanacetum, Teuricum mar, Zingiber

Active Ingredient(s):
  • 12 [hp_X]/59.1mL 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 GINGER;
  • 12 [hp_X]/59.1mL LYCOPODIUM CLAVATUM SPORE;
  • 12 [hp_X]/59.1mL MERCURIC CHLORIDE;
  • 12 [hp_X]/59.1mL 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 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


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Cell-mediated Immunity [PE];
  • Dietary Proteins [CS];
  • Food Additives [CS];
  • Increased Histamine Release [PE];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Plant Proteins [CS]

Labeler Information

Labeler Name: NET Remedies
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:12/4/2018

Package Information

No. Package Code Package Description Billing Unit
161626-0107-459 mL in 1 BOTTLE (61626-0107-4)

NDC Record

Field Name Field Value Definition
PRODUCT NDC61626-0107The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN PRESCRIPTION DRUGIndicates 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.
PROPRIETARY NAMEPara SolveThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMECalc carb, Chenopodium anth, Cina, Croton, Filix Mas, Gambocia, Granatum, Lycopodium, Merc corros, Nat phos, Santoninum, Senna, Spigelia anth, Stannum met, Tanacetum, Teuricum mar, ZingiberThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE12/4/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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.
LABELER NAMENET RemediesName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEARTEMISIA CINA PRE-FLOWERING TOP; CROTON TIGLIUM SEED; DRYOPTERIS FILIX-MAS ROOT; DYSPHANIA AMBROSIOIDES; GAMBOGE; GINGER; LYCOPODIUM CLAVATUM SPORE; MERCURIC CHLORIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PUNICA GRANATUM ROOT BARK; SANTONIN; SENNA LEAF; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SPIGELIA ANTHELMIA; TANACETUM VULGARE TOP; TEUCRIUM MARUM; TINAn 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.
ACTIVE NUMERATOR STRENGTH12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12 
ACTIVE INGRED UNIT[hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS] 

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This page was last updated on: 2/1/2023