83027-0090 NDC - FLU FORMULA (APIS MELLIFICA, ACONITUM NAPELLUS, ALLIUM CEPA, BRYONIA (ALBA), EUPATORIUM PERFOLIATUM, EUPHRASIA OFFICINALIS, IPECACUANHA, BELLADONNA, ECHINACEA PURPUREA, ASCLEPIAS VINCETOXICUM, GELSEMIUM SEMPERVIRENS, PHOSPHORUS, INFLUENZINUM)

Drug Information

  • Product NDC: 83027-0090
  • Proprietary Name: Flu Formula
  • Non Proprietary Name: Apis Mellifica, Aconitum Napellus, Allium Cepa, Bryonia (Alba), Eupatorium Perfoliatum, Euphrasia Officinalis, Ipecacuanha, Belladonna, Echinacea Purpurea, Asclepias Vincetoxicum, Gelsemium Sempervirens, Phosphorus, Influenzinum
  • Active Ingredient(s): 6 [hp_X]/mL ACONITUM NAPELLUS WHOLE; 6 [hp_X]/mL APIS MELLIFERA; 6 [hp_X]/mL ATROPA BELLADONNA; 6 [hp_X]/mL BRYONIA ALBA ROOT; 6 [hp_X]/mL ECHINACEA PURPUREA WHOLE; 6 [hp_X]/mL EUPATORIUM PERFOLIATUM FLOWERING TOP; 6 [hp_X]/mL EUPHRASIA STRICTA; 12 [hp_X]/mL GELSEMIUM SEMPERVIRENS ROOT; 12 [hp_X]/mL INFLUENZA A VIRUS A/DARWIN/9/2021 IVR-228 (H3N2) ANTIGEN (UV, FORMALDEHYDE INACTIVATED); 12 [hp_X]/mL INFLUENZA A VIRUS A/VICTORIA/2570/2019 IVR-215 (H1N1) ANTIGEN (UV, FORMALDEHYDE INACTIVATED); 12 [hp_X]/mL INFLUENZA B VIRUS B/AUSTRIA/1359417/2021 BVR-26 ANTIGEN (UV, FORMALDEHYDE INACTIVATED); 12 [hp_X]/mL INFLUENZA B VIRUS B/PHUKET/3073/2013 ANTIGEN (UV, FORMALDEHYDE INACTIVATED); 6 [hp_X]/mL IPECAC; 6 [hp_X]/mL ONION; 12 [hp_X]/mL PHOSPHORUS; 10 [hp_X]/mL VINCETOXICUM HIRUNDINARIA ROOT
  • Administration Route(s): ORAL
  • Dosage Form(s): SPRAY
  • Pharmacy Class(es): Allergens [CS]; Allergens [CS]; Bee Venoms [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Food Allergenic Extract [EPC]; Standardized Insect Venom Allergenic Extract [EPC]; Vegetable Proteins [CS]

Labeler Information

Field Name Field Value
Labeler Name: Nutritional Specialties, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:6/27/2023

Package Information

No. Package Code Package Description Billing Unit
183027-0090-160 mL in 1 BOTTLE, DROPPER (83027-0090-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC83027-0090The 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 NAMEFlu FormulaThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEApis Mellifica, Aconitum Napellus, Allium Cepa, Bryonia (Alba), Eupatorium Perfoliatum, Euphrasia Officinalis, Ipecacuanha, Belladonna, Echinacea Purpurea, Asclepias Vincetoxicum, Gelsemium Sempervirens, Phosphorus, InfluenzinumThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESPRAYThe 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 DATE6/27/2023This 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 NAMENutritional Specialties, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACONITUM NAPELLUS WHOLE; APIS MELLIFERA; ATROPA BELLADONNA; BRYONIA ALBA ROOT; ECHINACEA PURPUREA WHOLE; EUPATORIUM PERFOLIATUM FLOWERING TOP; EUPHRASIA STRICTA; GELSEMIUM SEMPERVIRENS ROOT; INFLUENZA A VIRUS A/DARWIN/9/2021 IVR-228 (H3N2) ANTIGEN (UV, FORMALDEHYDE INACTIVATED); INFLUENZA A VIRUS A/VICTORIA/2570/2019 IVR-215 (H1N1) ANTIGEN (UV, FORMALDEHYDE INACTIVATED); INFLUENZA B VIRUS B/AUSTRIA/1359417/2021 BVR-26 ANTIGEN (UV, FORMALDEHYDE INACTIVATED); INFLUENZA B VIRUS B/PHUKET/3073/2013 ANTIGEN (UV, FORMALDEHYDE INACTIVATED); IPECAC; ONION; PHOSPHORUS; VINCETOXICUM HIRUNDINARIA 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 STRENGTH6; 6; 6; 6; 6; 6; 6; 12; 12; 12; 12; 12; 6; 6; 12; 10 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAllergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Standardized Insect Venom Allergenic Extract [EPC], Vegetable Proteins [CS] 

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