Mercurius Combination Liquid
NDC 63083-9233
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
Mercurius Combination is a UNAPPROVED HOMEOPATHIC-approved product labeled by Professional Complementary Health Formulas. 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 63083-9233 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
63083-9233
Proprietary Name:
Mercurius Combination 9233
Non-Proprietary Name: [1]
Mercurius Combination
Substance Name: [2]
Ailanthus Altissima Flowering Twig; Amaryllis Belladonna Whole; Arsenic Trioxide; Calcium Sulfide; Daphne Mezereum Bark; Echinacea Angustifolia Whole; Human Herpesvirus 1; Lachesis Muta Venom; Mercurius Solubilis; Phytolacca Americana Root; Recombinant Varicella Zoster Virus Glycoprotein E Antigen
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:
63083
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]
08-15-1984
Listing Expiration Date: [11]
12-31-2027
Exclude Flag: [12]
N
Code Structure Chart
Product Details
What is NDC 63083-9233?
The NDC code 63083-9233 is assigned by the FDA to the product Mercurius Combination 9233. This pharmaceutical product is labeled by Professional Complementary Health Formulas 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: 63083-9233-1. 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?
For the temporary relief of acne, boils, or red, itchy, irritated skin.*
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.
- AILANTHUS ALTISSIMA FLOWERING TWIG 3 [hp_X]/29.5mL
- AMARYLLIS BELLADONNA WHOLE 4 [hp_X]/29.5mL
- ARSENIC TRIOXIDE 12 [hp_X]/29.5mL - 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.
- CALCIUM SULFIDE 8 [hp_X]/29.5mL - RN given refers to parent cpd; see also record for lime sulfur (calcium polysulfide)
- DAPHNE MEZEREUM BARK 9 [hp_X]/29.5mL
- ECHINACEA ANGUSTIFOLIA WHOLE 3 [hp_X]/29.5mL
- HUMAN HERPESVIRUS 1 12 [hp_X]/29.5mL - 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.
- LACHESIS MUTA VENOM 12 [hp_X]/29.5mL
- MERCURIUS SOLUBILIS 12 [hp_X]/29.5mL
- PHYTOLACCA AMERICANA ROOT 4 [hp_X]/29.5mL
- RECOMBINANT VARICELLA ZOSTER VIRUS GLYCOPROTEIN E ANTIGEN 12 [hp_X]/29.5mL
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- AILANTHUS ALTISSIMA FLOWERING TWIG (UNII: 8P29O5P7XU)
- AILANTHUS ALTISSIMA FLOWERING TWIG (UNII: 8P29O5P7XU) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8) (Active Moiety)
- AMARYLLIS BELLADONNA WHOLE (UNII: 11B89M58UN)
- AMARYLLIS BELLADONNA WHOLE (UNII: 11B89M58UN) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- HUMAN HERPESVIRUS 1 (UNII: 22G38P19RL)
- HUMAN HERPESVIRUS 1 (UNII: 22G38P19RL) (Active Moiety)
- RECOMBINANT VARICELLA ZOSTER VIRUS GLYCOPROTEIN E ANTIGEN (UNII: COB9FF6I46)
- RECOMBINANT VARICELLA ZOSTER VIRUS GLYCOPROTEIN E ANTIGEN (UNII: COB9FF6I46) (Active Moiety)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
* Please review the full disclaimer at the bottom of this page.
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".
