42681-9032 NDC - 365 EVERYDAY VALUE BE WELL COUGH EASE (ANTIMONY POTASSIUM TARTRATE, BRYONIA ALBA ROOT, PROTORTONIA CACTI, DROSERA ROTUNDIFOLIA, IPECAC, PULSATILLA VULGARIS, RUMEX CRISPUS ROOT, PONGIA OFFICINALIS SKELETON, ROASTED, LOBARIA PULMONARIA)

Drug Information

  • Product NDC: 42681-9032
  • Proprietary Name: 365 Everyday Value Be Well Cough Ease
  • Non Proprietary Name: ANTIMONY POTASSIUM TARTRATE, BRYONIA ALBA ROOT, PROTORTONIA CACTI, DROSERA ROTUNDIFOLIA, IPECAC, PULSATILLA VULGARIS, RUMEX CRISPUS ROOT, PONGIA OFFICINALIS SKELETON, ROASTED, LOBARIA PULMONARIA
  • Active Ingredient(s): 6 [hp_C]/mL ANTIMONY POTASSIUM TARTRATE; 3 [hp_C]/mL BRYONIA ALBA ROOT; 3 [hp_C]/mL DROSERA ROTUNDIFOLIA; 3 [hp_C]/mL IPECAC; 3 [hp_C]/mL LOBARIA PULMONARIA; 3 [hp_C]/mL PROTORTONIA CACTI; 6 [hp_C]/mL PULSATILLA VULGARIS; 6 [hp_C]/mL RUMEX CRISPUS ROOT; 3 [hp_C]/mL SPONGIA OFFICINALIS SKELETON, ROASTED
  • Administration Route(s): ORAL
  • Dosage Form(s): SYRUP

Labeler Information

Field Name Field Value
Labeler Name: WFM Private Label, LP
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:1/3/2011

Package Information

No. Package Code Package Description Billing Unit
142681-9032-1125 mL in 1 BOTTLE (42681-9032-1)
242681-9032-2200 mL in 1 BOTTLE (42681-9032-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC42681-9032The 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 NAME365 Everyday Value Be Well Cough EaseThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEANTIMONY POTASSIUM TARTRATE, BRYONIA ALBA ROOT, PROTORTONIA CACTI, DROSERA ROTUNDIFOLIA, IPECAC, PULSATILLA VULGARIS, RUMEX CRISPUS ROOT, PONGIA OFFICINALIS SKELETON, ROASTED, LOBARIA PULMONARIAThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESYRUPThe 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 DATE1/3/2011This 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 NAMEWFM Private Label, LPName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEANTIMONY POTASSIUM TARTRATE; BRYONIA ALBA ROOT; DROSERA ROTUNDIFOLIA; IPECAC; LOBARIA PULMONARIA; PROTORTONIA CACTI; PULSATILLA VULGARIS; RUMEX CRISPUS ROOT; SPONGIA OFFICINALIS SKELETON, ROASTEDAn 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 STRENGTH6; 3; 3; 3; 3; 3; 6; 6; 3 
ACTIVE INGRED UNIT[hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL 

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This page was last updated on: 11/21/2025

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