73421-2968 NDC - TOTAL FLU CLD 1 (ARSENICUM ALB, BAPTISIA, BRYONIA, CAUSTICUM, CINCHONA, DULCAMARA, ECHINACEA PURP, EUCALYPTUS, EUPATORIUM PERF, GELSEMIUM, INFLUENZINUM, LACHESIS, PHYTOLACCA, RHUS TOX, SARCOLACTICUM AC, SULPHUR, WYETHIA, ANAS BARBARIAE)

Drug Information

  • Product NDC: 73421-2968
  • Proprietary Name: TOTAL FLU CLD 1
  • Non Proprietary Name: Arsenicum alb, Baptisia, Bryonia, Causticum, Cinchona, Dulcamara, Echinacea purp, Eucalyptus, Eupatorium perf, Gelsemium, Influenzinum, Lachesis, Phytolacca, Rhus tox, Sarcolacticum ac, Sulphur, Wyethia, Anas barbariae
  • Active Ingredient(s): 10 [hp_X]/29.6mL ARSENIC TRIOXIDE; 10 [hp_X]/29.6mL BAPTISIA TINCTORIA ROOT; 10 [hp_X]/29.6mL BRYONIA ALBA ROOT; 35 [hp_C]/29.6mL CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE; 10 [hp_X]/29.6mL CAUSTICUM; 10 [hp_X]/29.6mL CINCHONA BARK; 10 [hp_X]/29.6mL ECHINACEA PURPUREA; 10 [hp_X]/29.6mL EUCALYPTUS GLOBULUS LEAF; 10 [hp_X]/29.6mL EUPATORIUM PERFOLIATUM FLOWERING TOP; 10 [hp_X]/29.6mL GELSEMIUM SEMPERVIRENS ROOT; 10 [hp_X]/29.6mL INFLUENZA A VIRUS; 10 [hp_X]/29.6mL LACHESIS MUTA VENOM; 10 [hp_X]/29.6mL LACTIC ACID, L-; 10 [hp_X]/29.6mL PHYTOLACCA AMERICANA ROOT; 10 [hp_X]/29.6mL SOLANUM DULCAMARA TOP; 10 [hp_X]/29.6mL SULFUR; 10 [hp_X]/29.6mL TOXICODENDRON PUBESCENS LEAF; 10 [hp_X]/29.6mL WYETHIA HELENIOIDES ROOT
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID

Labeler Information

Field Name Field Value
Labeler Name: White Manufacturing Inc. DBA Micro-West
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:6/1/2021

Package Information

No. Package Code Package Description Billing Unit
173421-2968-129.6 mL in 1 BOTTLE (73421-2968-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC73421-2968The 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 NAMETOTAL FLU CLD 1The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEArsenicum alb, Baptisia, Bryonia, Causticum, Cinchona, Dulcamara, Echinacea purp, Eucalyptus, Eupatorium perf, Gelsemium, Influenzinum, Lachesis, Phytolacca, Rhus tox, Sarcolacticum ac, Sulphur, Wyethia, Anas barbariaeThe 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 DATE6/1/2021This 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 NAMEWhite Manufacturing Inc. DBA Micro-WestName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEARSENIC TRIOXIDE; BAPTISIA TINCTORIA ROOT; BRYONIA ALBA ROOT; CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE; CAUSTICUM; CINCHONA BARK; ECHINACEA PURPUREA; EUCALYPTUS GLOBULUS LEAF; EUPATORIUM PERFOLIATUM FLOWERING TOP; GELSEMIUM SEMPERVIRENS ROOT; INFLUENZA A VIRUS; LACHESIS MUTA VENOM; LACTIC ACID, L-; PHYTOLACCA AMERICANA ROOT; SOLANUM DULCAMARA TOP; SULFUR; TOXICODENDRON PUBESCENS LEAF; WYETHIA HELENIOIDES ROOTAn 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 STRENGTH10; 10; 10; 35; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10 
ACTIVE INGRED UNIT[hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_C]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL 

Download Record

Download this NDC record record in Text format: Export

Download this NDC record record in Excel (CSV) format: Export

Download this NDC record record in XML format: Export

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

Previous Code
Next Code