Vacc Hc Liquid
NDC 43742-2152
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
Vacc Hc (antimonium tartaricum, arsenicum album, bryonia (alba), echinacea (angustifolia), gelsemium sempervirens, hepar suis, histaminum hydrochloricum, hyoscyamus niger, influenzinum, lac felinum, ledum palustre, mercurius solubilis, mezereum, nicotinamidum, rna, senega officinalis, silicea, spigelia anthelmia, sulphur, thuja occidentalis, zincum metallicum.) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Deseret Biologicals, Inc.. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 43742-2152 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
43742-2152
Proprietary Name:
Vacc Hc
Non-Proprietary Name: [1]
Antimonium Tartaricum, Arsenicum Album, Bryonia (alba), Echinacea (angustifolia), Gelsemium Sempervirens, Hepar Suis, Histaminum Hydrochloricum, Hyoscyamus Niger, Influenzinum, Lac Felinum, Ledum Palustre, Mercurius Solubilis, Mezereum, Nicotinamidum, Rna, Senega Officinalis, Silicea, Spigelia Anthelmia, Sulphur, Thuja Occidentalis, Zincum Metallicum.
Substance Name: [2]
Antimony Potassium Tartrate; Arsenic Trioxide; Bryonia Alba Root; Daphne Mezereum Bark; Echinacea Angustifolia Whole; Felis Catus Milk; Gelsemium Sempervirens Root; Histamine Dihydrochloride; Hyoscyamus Niger; Influenza A Virus A/darwin/6/2021 (h3n2) Whole; Influenza A Virus Whole; Influenza B Virus B/austria/1359417/2021 Bvr-26 Whole; Influenza B Virus B/phuket/3073/2013 Bvr-1b Whole; Mercurius Solubilis; Niacinamide; Polygala Senega Root; Pork Liver; Rhododendron Tomentosum Leafy Twig; Saccharomyces Cerevisiae Rna; Silicon Dioxide; Spigelia Anthelmia Whole; Sulfur; Thuja Occidentalis Leafy Twig; Zinc
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]
04-23-2024
End Marketing Date: [10]
06-10-2029
Exclude Flag: [12]
N
Code Structure Chart
Product Details
What is NDC 43742-2152?
The NDC code 43742-2152 is assigned by the FDA to the product Vacc Hc. It is commonly known by its generic name, antimonium tartaricum, arsenicum album, bryonia (alba), echinacea (angustifolia), gelsemium sempervirens, hepar suis, histaminum hydrochloricum, hyoscyamus niger, influenzinum, lac felinum, ledum palustre, mercurius solubilis, mezereum, nicotinamidum, rna, senega officinalis, silicea, spigelia anthelmia, sulphur, thuja occidentalis, zincum metallicum.. 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: 43742-2152-1. 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.
- ANTIMONY POTASSIUM TARTRATE 30 [hp_X]/mL - A schistosomicide possibly useful against other parasites. It has irritant emetic properties and may cause lethal cardiac toxicity among other adverse effects.
- ARSENIC TRIOXIDE 30 [hp_X]/mL - 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.
- BRYONIA ALBA ROOT 30 [hp_X]/mL
- DAPHNE MEZEREUM BARK 12 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA WHOLE 12 [hp_X]/mL
- FELIS CATUS MILK 30 [hp_X]/mL
- GELSEMIUM SEMPERVIRENS ROOT 30 [hp_X]/mL
- HISTAMINE DIHYDROCHLORIDE 6 [hp_X]/mL - An amine derived by enzymatic decarboxylation of HISTIDINE. It is a powerful stimulant of gastric secretion, a constrictor of bronchial smooth muscle, a vasodilator, and also a centrally acting neurotransmitter.
- HYOSCYAMUS NIGER 30 [hp_X]/mL - A plant genus of the family SOLANACEAE which contains TROPANES.
- INFLUENZA A VIRUS A/DARWIN/6/2021 (H3N2) WHOLE 12 [hp_C]/mL
- INFLUENZA A VIRUS WHOLE 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
- MERCURIUS SOLUBILIS 30 [hp_X]/mL
- NIACINAMIDE 30 [hp_X]/mL - An important compound functioning as a component of the coenzyme NAD. Its primary significance is in the prevention and/or cure of blacktongue and PELLAGRA. Most animals cannot manufacture this compound in amounts sufficient to prevent nutritional deficiency and it therefore must be supplemented through dietary intake.
- POLYGALA SENEGA ROOT 30 [hp_X]/mL
- PORK LIVER 6 [hp_X]/mL
- RHODODENDRON TOMENTOSUM LEAFY TWIG 12 [hp_X]/mL
- SACCHAROMYCES CEREVISIAE RNA 10 [hp_X]/mL
- SILICON DIOXIDE 12 [hp_X]/mL - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
- SPIGELIA ANTHELMIA WHOLE 30 [hp_X]/mL
- SULFUR 30 [hp_X]/mL - 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.
- THUJA OCCIDENTALIS LEAFY TWIG 6 [hp_X]/mL
- ZINC 30 [hp_X]/mL - A metallic element of atomic number 30 and atomic weight 65.38. It is a necessary trace element in the diet, forming an essential part of many enzymes, and playing an important role in protein synthesis and in cell division. Zinc deficiency is associated with ANEMIA, short stature, HYPOGONADISM, impaired WOUND HEALING, and geophagia. It is known by the symbol Zn.
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3)
- ANTIMONY CATION (3+) (UNII: 069647RPT5) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- PORK LIVER (UNII: 6EC706HI7F)
- PORK LIVER (UNII: 6EC706HI7F) (Active Moiety)
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
- HYOSCYAMUS NIGER (UNII: 4WRK2153H3)
- HYOSCYAMUS NIGER (UNII: 4WRK2153H3) (Active Moiety)
- INFLUENZA A VIRUS WHOLE (UNII: R9HH0NDE2E)
- INFLUENZA A VIRUS WHOLE (UNII: R9HH0NDE2E) (Active Moiety)
- INFLUENZA A VIRUS A/DARWIN/6/2021 (H3N2) WHOLE (UNII: PMY5J4Z7LS)
- INFLUENZA A VIRUS A/DARWIN/6/2021 (H3N2) WHOLE (UNII: PMY5J4Z7LS) (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)
- FELIS CATUS MILK (UNII: 5A3Y60049Z)
- FELIS CATUS MILK (UNII: 5A3Y60049Z) (Active Moiety)
- RHODODENDRON TOMENTOSUM LEAFY TWIG (UNII: 877L01IZ0P)
- LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (Active Moiety)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (Active Moiety)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- SACCHAROMYCES CEREVISIAE RNA (UNII: J17GBZ5VGX)
- SACCHAROMYCES CEREVISIAE RNA (UNII: J17GBZ5VGX) (Active Moiety)
- POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF)
- POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- SPIGELIA ANTHELMIA WHOLE (UNII: WYT05213GE)
- SPIGELIA ANTHELMIA (UNII: WYT05213GE) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
- ZINC (UNII: J41CSQ7QDS)
- ZINC (UNII: J41CSQ7QDS) (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)
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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 End Marketing Date? This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
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".
