Vir Combination Liquid
NDC 43742-2539
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
Vir Combination (adenoviren nosode, cytomegalovirus nosode, herpes simplex virus 1 and 2 dna, epstein-barr virus nosode, hepatitis b nosode, herpes simplex i and ii nosode, human herpesvirus 6a, human herpesvirus 6b, influenzinum) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Deseret Biologicals, Inc.. This medication is typically used as a actively acquired immunity [pe]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 43742-2539 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
43742-2539
Proprietary Name:
Vir Combination
Non-Proprietary Name: [1]
Adenoviren Nosode, Cytomegalovirus Nosode, Herpes Simplex Virus 1 And 2 Dna, Epstein-barr Virus Nosode, Hepatitis B Nosode, Herpes Simplex I And Ii Nosode, Human Herpesvirus 6a, Human Herpesvirus 6b, Influenzinum
Substance Name: [2]
Hepatitis B Virus; Herring Sperm Dna; Human Adenovirus E Serotype 4 Strain Cl-68578 Antigen; Human Herpesvirus 1; Human Herpesvirus 2; Human Herpesvirus 4; Human Herpesvirus 5; Human Herpesvirus 6; Influenza A Virus A/thailand/8/2022 Ivr-237 (h3n2) Antigen (formaldehyde Inactivated); Influenza A Virus A/victoria/4897/2022 Ivr-238 (h1n1) Antigen (formaldehyde Inactivated); Influenza B Virus B/austria/1359417/2021 Bvr-26 Whole; Influenza B Virus B/phuket/3073/2013 Bvr-1b Whole
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:
43742
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]
03-26-2026
Listing Expiration Date: [11]
12-31-2027
Exclude Flag: [12]
N
Code Structure Chart
Product Details
What is NDC 43742-2539?
The NDC code 43742-2539 is assigned by the FDA to the product Vir Combination. It is commonly known by its generic name, adenoviren nosode, cytomegalovirus nosode, herpes simplex virus 1 and 2 dna, epstein-barr virus nosode, hepatitis b nosode, herpes simplex i and ii nosode, human herpesvirus 6a, human herpesvirus 6b, influenzinum. This pharmaceutical product is labeled by Deseret Biologicals, 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: 43742-2539-1. 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?
1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.
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.
- HEPATITIS B VIRUS 33 [hp_X]/mL - The type species of the genus ORTHOHEPADNAVIRUS which causes human HEPATITIS B and is also apparently a causal agent in human HEPATOCELLULAR CARCINOMA. The Dane particle is an intact hepatitis virion, named after its discoverer. Non-infectious spherical and tubular particles are also seen in the serum.
- HERRING SPERM DNA 12 [hp_X]/mL
- HUMAN ADENOVIRUS E SEROTYPE 4 STRAIN CL-68578 ANTIGEN 12 [hp_C]/mL
- HUMAN HERPESVIRUS 1 15 [hp_X]/mL - The type species of SIMPLEXVIRUS causing most forms of non-genital herpes simplex in humans. Primary infection occurs mainly in infants and young children and then the virus becomes latent in the dorsal root ganglion. It then is periodically reactivated throughout life causing mostly benign conditions.
- HUMAN HERPESVIRUS 2 15 [hp_X]/mL
- HUMAN HERPESVIRUS 4 16 [hp_C]/mL
- HUMAN HERPESVIRUS 5 18 [hp_X]/mL
- HUMAN HERPESVIRUS 6 15 [hp_X]/mL - Members of the ROSEOLOVIRUS genus of the Betaherpesvirales subfamily isolated from patients with AIDS and other LYMPHOPROLIFERATIVE DISORDERS. It infects and replicates in fresh and established lines of hematopoietic cells and cells of neural origin. It also appears to alter the activity of NK CELLS. HHV-6; (HBLV) antibodies are elevated in patients with AIDS; SJOGREN'S SYNDROME; SARCOIDOSIS; CHRONIC FATIGUE SYNDROME, and certain malignancies. HHV-6A is the most common cause of EXANTHEMA SUBITUM and has been implicated in encephalitis. When HHV-6 integrates into the host genome it is referred to as ciHVH-6. When such VIRUS INTEGRATION occurs into the germline it is referred to as iciHHV-6.
- INFLUENZA A VIRUS A/THAILAND/8/2022 IVR-237 (H3N2) ANTIGEN (FORMALDEHYDE INACTIVATED) 12 [hp_C]/mL
- INFLUENZA A VIRUS A/VICTORIA/4897/2022 IVR-238 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED) 12 [hp_C]/mL
- INFLUENZA B VIRUS B/AUSTRIA/1359417/2021 BVR-26 WHOLE 12 [hp_C]/mL
- INFLUENZA B VIRUS B/PHUKET/3073/2013 BVR-1B WHOLE 12 [hp_C]/mL
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- HUMAN ADENOVIRUS E SEROTYPE 4 STRAIN CL-68578 ANTIGEN (UNII: FKD3DUK39I)
- HUMAN ADENOVIRUS E SEROTYPE 4 STRAIN CL-68578 (UNII: FKD3DUK39I) (Active Moiety)
- HUMAN HERPESVIRUS 5 (UNII: 7COI029E6K)
- HUMAN HERPESVIRUS 5 (UNII: 7COI029E6K) (Active Moiety)
- HERRING SPERM DNA (UNII: 51FI676N6F)
- HERRING SPERM DNA (UNII: 51FI676N6F) (Active Moiety)
- HUMAN HERPESVIRUS 4 (UNII: 2A26YW7PNX)
- HUMAN HERPESVIRUS 4 (UNII: 2A26YW7PNX) (Active Moiety)
- HEPATITIS B VIRUS (UNII: 77H9EM77P7)
- HEPATITIS B VIRUS (UNII: 77H9EM77P7) (Active Moiety)
- HUMAN HERPESVIRUS 1 (UNII: 22G38P19RL)
- HUMAN HERPESVIRUS 1 (UNII: 22G38P19RL) (Active Moiety)
- HUMAN HERPESVIRUS 2 (UNII: 74J6DNH49U)
- HUMAN HERPESVIRUS 2 (UNII: 74J6DNH49U) (Active Moiety)
- HUMAN HERPESVIRUS 6 (UNII: 4IX4VP35CR)
- HUMAN HERPESVIRUS 6 (UNII: 4IX4VP35CR) (Active Moiety)
- INFLUENZA A VIRUS A/VICTORIA/4897/2022 IVR-238 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: AU5C98U4BB)
- INFLUENZA A VIRUS A/VICTORIA/4897/2022 IVR-238 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: AU5C98U4BB) (Active Moiety)
- INFLUENZA A VIRUS A/THAILAND/8/2022 IVR-237 (H3N2) ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 6TU4EY6UNW)
- INFLUENZA A VIRUS A/THAILAND/8/2022 IVR-237 (H3N2) ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 6TU4EY6UNW) (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 BVR-1B WHOLE (UNII: PS2DCE2WVF)
- INFLUENZA B VIRUS B/PHUKET/3073/2013 BVR-1B WHOLE (UNII: PS2DCE2WVF) (Active Moiety)
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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
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.
- Actively Acquired Immunity - [PE] (Physiologic Effect)
- Live Human Adenovirus Type 4 Vaccine - [EPC] (Established Pharmacologic Class)
- Vaccines, Adenovirus - [Chemical/Ingredient]
- Vaccines, Live, Unattenuated - [Chemical/Ingredient]
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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".
