66096-709 NDC - COUGH RELIEF SYRUP (ALTHAEA, ANTIMON SULPH, ANTIMON TART, BRYONIA, CETRARIA, CHAMOMILLA, DROSERA, ECHINACEA ANG, IPECAC, KALI MUR, PLANTAGO, RUMEX CRISP, SENEGA, SPONGIA, THYMUS, TRIFOLIUM PRAT, URTICA DI, VERBASCUM.)

Drug Information

Product NDC: 66096-709

Proprietary Name: Cough Relief Syrup

Non Proprietary Name: Althaea, Antimon Sulph, Antimon Tart, Bryonia, Cetraria, Chamomilla, Drosera, Echinacea Ang, Ipecac, Kali Mur, Plantago, Rumex Crisp, Senega, Spongia, Thymus, Trifolium Prat, Urtica Di, Verbascum.

Active Ingredient(s):
  • 1 [hp_X]/148mL ALTHAEA OFFICINALIS ROOT;
  • 12 [hp_X]/148mL ANTIMONY PENTASULFIDE;
  • 6 [hp_X]/148mL ANTIMONY POTASSIUM TARTRATE;
  • 6 [hp_X]/148mL BRYONIA ALBA ROOT;
  • 1 [hp_X]/148mL CETRARIA ISLANDICA SUBSP. ISLANDICA;
  • 6 [hp_X]/148mL DROSERA ROTUNDIFOLIA;
  • 1 [hp_X]/148mL ECHINACEA ANGUSTIFOLIA;
  • 6 [hp_X]/148mL IPECAC;
  • 1 [hp_X]/148mL MATRICARIA RECUTITA;
  • 1 [hp_X]/148mL PLANTAGO LANCEOLATA POLLEN;
  • 6 [hp_X]/148mL POLYGALA SENEGA ROOT;
  • 6 [hp_X]/148mL POTASSIUM CHLORIDE;
  • 6 [hp_X]/148mL RUMEX CRISPUS ROOT;
  • 6 [hp_X]/148mL SPONGIA OFFICINALIS SKELETON, ROASTED;
  • 1 [hp_X]/148mL SUS SCROFA THYMUS;
  • 1 [hp_X]/148mL TRIFOLIUM PRATENSE FLOWER;
  • 1 [hp_X]/148mL URTICA DIOICA;
  • 1 [hp_X]/148mL VERBASCUM THAPSUS


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Cell-mediated Immunity [PE];
  • Increased Histamine Release [PE];
  • Increased IgG Production [PE];
  • Increased Large Intestinal Motility [PE];
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE];
  • Non-Standardized Pollen Allergenic Extract [EPC];
  • Osmotic Activity [MoA];
  • Osmotic Laxative [EPC];
  • Pollen [CS];
  • Potassium Compounds [CS];
  • Potassium Salt [EPC]

Labeler Information

Labeler Name: OHM PHARMA INC.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:8/18/2015

Package Information

No. Package Code Package Description Billing Unit
166096-709-25148 mL in 1 BOTTLE (66096-709-25)

NDC Record

Field Name Field Value Definition
PRODUCT NDC66096-709The 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 OTC 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 NAMECough Relief SyrupThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAlthaea, Antimon Sulph, Antimon Tart, Bryonia, Cetraria, Chamomilla, Drosera, Echinacea Ang, Ipecac, Kali Mur, Plantago, Rumex Crisp, Senega, Spongia, Thymus, Trifolium Prat, Urtica Di, Verbascum.The 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 DATE8/18/2015This 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 NAMEOHM PHARMA INC.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEALTHAEA OFFICINALIS ROOT; ANTIMONY PENTASULFIDE; ANTIMONY POTASSIUM TARTRATE; BRYONIA ALBA ROOT; CETRARIA ISLANDICA SUBSP. ISLANDICA; DROSERA ROTUNDIFOLIA; ECHINACEA ANGUSTIFOLIA; IPECAC; MATRICARIA RECUTITA; PLANTAGO LANCEOLATA POLLEN; POLYGALA SENEGA ROOT; POTASSIUM CHLORIDE; RUMEX CRISPUS ROOT; SPONGIA OFFICINALIS SKELETON, ROASTED; SUS SCROFA THYMUS; TRIFOLIUM PRATENSE FLOWER; URTICA DIOICA; VERBASCUM THAPSUSAn 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 STRENGTH1; 12; 6; 6; 1; 6; 1; 6; 1; 1; 6; 6; 6; 6; 1; 1; 1; 1 
ACTIVE INGRED UNIT[hp_X]/148mL; [hp_X]/148mL; [hp_X]/148mL; [hp_X]/148mL; [hp_X]/148mL; [hp_X]/148mL; [hp_X]/148mL; [hp_X]/148mL; [hp_X]/148mL; [hp_X]/148mL; [hp_X]/148mL; [hp_X]/148mL; [hp_X]/148mL; [hp_X]/148mL; [hp_X]/148mL; [hp_X]/148mL; [hp_X]/148mL; [hp_X]/148mL 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Non-Standardized Pollen Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Pollen [CS], Potassium Compounds [CS], Potassium Salt [EPC] 

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