57955-9987 NDC - MULTI-STRAIN COLD AND FLU RELIEF (ANAS BARBARIAE (35C, 50C, 100C, 200C), ARSENICUM ALB, BAPTISIA, BRYONIA, CAUSTICUM, CINCHONA, ECHINACEA PURP, EUCALYPTUS, EUPATORIUM PERF, GELSEMIUM, INFLUENZINUM, PHYTOLACCA, RHUS TOX, SARCOLACTICUM AC, SULPHUR, WYETHIA, ZINC ACET, ZINC MUR, AND ZINC OXYD.)

Drug Information

  • Product NDC: 57955-9987
  • Proprietary Name: Multi-Strain Cold and Flu Relief
  • Non Proprietary Name: Anas barbariae (35C, 50C, 100C, 200C), Arsenicum alb, Baptisia, Bryonia, Causticum, Cinchona, Echinacea purp, Eucalyptus, Eupatorium perf, Gelsemium, Influenzinum, Phytolacca, Rhus tox, Sarcolacticum ac, Sulphur, Wyethia, Zinc acet, Zinc mur, and Zinc oxyd.
  • Active Ingredient(s): 10 [hp_X]/59mL ARSENIC TRIOXIDE; 10 [hp_X]/59mL BAPTISIA TINCTORIA ROOT; 10 [hp_X]/59mL BRYONIA ALBA ROOT; 35 [hp_C]/59mL CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE; 10 [hp_X]/59mL CAUSTICUM; 10 [hp_X]/59mL CINCHONA OFFICINALIS BARK; 10 [hp_X]/59mL ECHINACEA PURPUREA WHOLE; 10 [hp_X]/59mL EUCALYPTUS GLOBULUS LEAF; 10 [hp_X]/59mL EUPATORIUM PERFOLIATUM FLOWERING TOP; 10 [hp_X]/59mL GELSEMIUM SEMPERVIRENS ROOT; 10 [hp_X]/59mL INFLUENZA A VIRUS A/DARWIN/9/2021 SAN-010 (H3N2) HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED); 10 [hp_X]/59mL INFLUENZA A VIRUS A/VICTORIA/4897/2022 IVR-238 (H1N1) HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED); 10 [hp_X]/59mL INFLUENZA B VIRUS B/AUSTRIA/1359417/2021 BVR-26 WHOLE; 10 [hp_X]/59mL INFLUENZA B VIRUS B/PHUKET/3073/2013 RECOMBINANT HEMAGGLUTININ ANTIGEN; 10 [hp_X]/59mL LACTIC ACID, L-; 10 [hp_X]/59mL PHYTOLACCA AMERICANA ROOT; 10 [hp_X]/59mL SULFUR; 10 [hp_X]/59mL TOXICODENDRON PUBESCENS LEAF; 10 [hp_X]/59mL WYETHIA HELENIOIDES ROOT; 10 [hp_X]/59mL ZINC ACETATE ANHYDROUS; 10 [hp_X]/59mL ZINC CHLORIDE; 10 [hp_X]/59mL ZINC OXIDE
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Copper Absorption Inhibitor [EPC]; Copper Absorption Inhibitor [EPC]; Copper Absorption Inhibitor [EPC]; Decreased Copper Ion Absorption [PE]; Decreased Copper Ion Absorption [PE]; Decreased Copper Ion Absorption [PE]

Labeler Information

Field Name Field Value
Labeler Name: King Bio Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:3/10/2026

Package Information

No. Package Code Package Description Billing Unit
157955-9987-259 mL in 1 BOTTLE, SPRAY (57955-9987-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC57955-9987The 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 NAMEMulti-Strain Cold and Flu ReliefThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAnas barbariae (35C, 50C, 100C, 200C), Arsenicum alb, Baptisia, Bryonia, Causticum, Cinchona, Echinacea purp, Eucalyptus, Eupatorium perf, Gelsemium, Influenzinum, Phytolacca, Rhus tox, Sarcolacticum ac, Sulphur, Wyethia, Zinc acet, Zinc mur, and Zinc oxyd.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 DATE3/10/2026This 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 NAMEKing Bio Inc.Name 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 OFFICINALIS BARK; ECHINACEA PURPUREA WHOLE; EUCALYPTUS GLOBULUS LEAF; EUPATORIUM PERFOLIATUM FLOWERING TOP; GELSEMIUM SEMPERVIRENS ROOT; INFLUENZA A VIRUS A/DARWIN/9/2021 SAN-010 (H3N2) HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED); INFLUENZA A VIRUS A/VICTORIA/4897/2022 IVR-238 (H1N1) HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED); INFLUENZA B VIRUS B/AUSTRIA/1359417/2021 BVR-26 WHOLE; INFLUENZA B VIRUS B/PHUKET/3073/2013 RECOMBINANT HEMAGGLUTININ ANTIGEN; LACTIC ACID, L-; PHYTOLACCA AMERICANA ROOT; SULFUR; TOXICODENDRON PUBESCENS LEAF; WYETHIA HELENIOIDES ROOT; ZINC ACETATE ANHYDROUS; ZINC CHLORIDE; ZINC OXIDEAn 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; 10; 10; 10; 10 
ACTIVE INGRED UNIT[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_C]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL 
PHARM CLASSESCopper Absorption Inhibitor [EPC], Copper Absorption Inhibitor [EPC], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Decreased Copper Ion Absorption [PE], Decreased Copper Ion Absorption [PE] 

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This page was last updated on: 3/27/2026

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