Multi-strain Cold And Flu Relief Liquid
NDC 57955-9987
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
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.) is a UNAPPROVED HOMEOPATHIC-approved product labeled by King Bio Inc.. This medication is typically used as a copper absorption inhibitor [epc]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 57955-9987 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
57955-9987
Proprietary Name:
Multi-strain Cold And Flu Relief
Non-Proprietary Name: [1]
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.
Substance Name: [2]
Arsenic 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 Oxide
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:
Clinical Specifications
Dosage Form:
Liquid
- A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler & Regulatory Data
Labeler Name: [5]
Labeler Code:
57955
Product Label ID:
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Marketing Timeline
Start Marketing Date: [9]
03-10-2026
Listing Expiration Date: [11]
12-31-2027
Exclude Flag: [12]
N
Code Structure Chart
Product Details
What is NDC 57955-9987?
The NDC code 57955-9987 is assigned by the FDA to the product Multi-strain Cold And Flu Relief. It is commonly known by its generic 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.. This pharmaceutical product is labeled by King Bio Inc. and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 57955-9987-2. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.
What are the uses of this product?
Uses † temporarily relief of:feverchillsbody achesnauseafatigueheadachesneezingrunny nosenasal congestioncoughdiarrheanight sweatsvomitinghead coldsmucus congestion † Claims based on traditional Homeopathic practice, not accepted medical evidence, notFDA evaluated.
What are Active Ingredients of this product?
An 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.
- ARSENIC TRIOXIDE 10 [hp_X]/59mL - An inorganic compound with the chemical formula As2O3 that is used for the treatment of ACUTE PROMYELOCYTIC LEUKEMIA in patients who have relapsed from, or are resistant to, conventional drug therapy.
- BAPTISIA TINCTORIA ROOT 10 [hp_X]/59mL
- BRYONIA ALBA ROOT 10 [hp_X]/59mL
- CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE 35 [hp_C]/59mL
- CAUSTICUM 10 [hp_X]/59mL - contains calcium hydroxide & potassium bisulfite; Homeopathic drug
- 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 - An element that is a member of the chalcogen family. It has an atomic symbol S, atomic number 16, and atomic weight [32.059; 32.076]. It is found in the amino acids cysteine and methionine.
- TOXICODENDRON PUBESCENS LEAF 10 [hp_X]/59mL
- WYETHIA HELENIOIDES ROOT 10 [hp_X]/59mL
- ZINC ACETATE ANHYDROUS 10 [hp_X]/59mL - A salt produced by the reaction of zinc oxide with acetic acid and used as an astringent, styptic, and emetic.
- ZINC CHLORIDE 10 [hp_X]/59mL - RN given refers to parent cpd
- ZINC OXIDE 10 [hp_X]/59mL - A mild astringent and topical protectant with some antiseptic action. It is also used in bandages, pastes, ointments, dental cements, and as a sunblock.
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY)
- CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU)
- BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- CAUSTICUM (UNII: DD5FO1WKFU)
- CAUSTICUM (UNII: DD5FO1WKFU) (Active Moiety)
- CINCHONA OFFICINALIS BARK (UNII: S003A158SB)
- CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (Active Moiety)
- ECHINACEA PURPUREA WHOLE (UNII: QI7G114Y98)
- ECHINACEA PURPUREA (UNII: QI7G114Y98) (Active Moiety)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (Active Moiety)
- EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E)
- EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- INFLUENZA A VIRUS A/VICTORIA/4897/2022 IVR-238 (H1N1) HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: C46XJT9FQ9)
- INFLUENZA A VIRUS A/VICTORIA/4897/2022 IVR-238 (H1N1) HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: C46XJT9FQ9) (Active Moiety)
- INFLUENZA A VIRUS A/DARWIN/9/2021 SAN-010 (H3N2) HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 6S4Y8A8UEY)
- INFLUENZA A VIRUS A/DARWIN/9/2021 SAN-010 (H3N2) HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 6S4Y8A8UEY) (Active Moiety)
- INFLUENZA B VIRUS B/AUSTRIA/1359417/2021 BVR-26 WHOLE (UNII: CYK5P89K8X)
- INFLUENZA B VIRUS B/AUSTRIA/1359417/2021 BVR-26 WHOLE (UNII: CYK5P89K8X) (Active Moiety)
- INFLUENZA B VIRUS B/PHUKET/3073/2013 RECOMBINANT HEMAGGLUTININ ANTIGEN (UNII: POQ8DQO9S3)
- INFLUENZA B VIRUS B/PHUKET/3073/2013 RECOMBINANT HEMAGGLUTININ ANTIGEN (UNII: POQ8DQO9S3) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- LACTIC ACID, L- (UNII: F9S9FFU82N)
- LACTIC ACID, L- (UNII: F9S9FFU82N) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N)
- WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N) (Active Moiety)
- ZINC ACETATE ANHYDROUS (UNII: H2ZEY72PME)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- ZINC CHLORIDE (UNII: 86Q357L16B)
- ZINC OXIDE (UNII: SOI2LOH54Z)
Which are the Inactive Ingredients associated UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WATER (UNII: 059QF0KO0R)
Which are the Pharmacologic Classes of this product?
A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.
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Product & Regulatory Definitions
What is the Non-Proprietary Name? The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
What is the Substance Name? An 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.
What kind of product is this? Indicates 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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the Marketing Category? Product 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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
What is the Listing Expiration Date? This is the date when the listing record will expire if not updated or certified by the product labeler.
What is the NDC Exclude Flag? This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".
