Unda 48

Condurango, Calendula Officinalis, Lycopodium Clavatum, Sabina, Thuja Occidentalis, Aurum Metallicum, Plumbum Metallicum, Arsenicum Album

Seroyal Usa
Human Otc Drug
NDC 62106-1147

Unda 48 also known as Condurango, Calendula Officinalis, Lycopodium Clavatum, Sabina, Thuja Occidentalis, Aurum Metallicum, Plumbum Metallicum, Arsenicum Album is a human otc drug labeled by 'Seroyal Usa'. National Drug Code (NDC) number for Unda 48 is 62106-1147. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Unda 48 drug includes Arsenic Trioxide - 12 [hp_X]/20mL Calendula Officinalis Flowering Top - 4 [hp_X]/20mL Gold - 12 [hp_X]/20mL Juniperus Sabina Leaf - 4 [hp_X]/20mL Lead - 12 [hp_X]/20mL Lycopodium Clavatum Spore - 4 [hp_X]/20mL Marsdenia Condurango Bark - 4 [hp_X]/20mL Thuja Occidentalis Leafy Twig - 4 [hp_X]/20mL . The currest status of Unda 48 drug is Active.

Drug Information:

Drug NDC:	62106-1147
The 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.
Proprietary Name:	Unda 48
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name:	Condurango, Calendula Officinalis, Lycopodium Clavatum, Sabina, Thuja Occidentalis, Aurum Metallicum, Plumbum Metallicum, Arsenicum Album
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Seroyal Usa
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Liquid
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	ARSENIC TRIOXIDE - 12 [hp_X]/20mL CALENDULA OFFICINALIS FLOWERING TOP - 4 [hp_X]/20mL GOLD - 12 [hp_X]/20mL JUNIPERUS SABINA LEAF - 4 [hp_X]/20mL LEAD - 12 [hp_X]/20mL LYCOPODIUM CLAVATUM SPORE - 4 [hp_X]/20mL MARSDENIA CONDURANGO BARK - 4 [hp_X]/20mL THUJA OCCIDENTALIS LEAFY TWIG - 4 [hp_X]/20mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	08 May, 2015
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	24 Dec, 2025
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.
Listing Expiration Date:	31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Seroyal USA
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
UPC:	0883196301102
UPC stands for Universal Product Code.
NUI:	N0000185508 N0000175629 N0000184306 M0000728 N0000185375 N0000185001 M0016962
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	Q4EWM09M3O CPD4NFA903 74068FOS7R 79Y1949PYO 38SNL0F81Z R23QIR6YBA 9Q24RAI43V 9IH82J936J 1NT28V9397 464910T5N9 Load more... 18E7415PXQ C88X29Y479 3M4G523W1G KPS1B1162N G0R4UBI2ZZ W1LUS9R48G XZC6H8R666 1DP6Y6B65Z 3M5V3D1X36 6D74QW4H67 S7V92P67HO 75O014T1HG M7T6H7D4IF E678D1QH0K 2FXJ6SW4PK 387GMG9FH5 0R715588D2 2P299V784P
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class EPC:	Standardized Chemical Allergen [EPC] Non-Standardized Plant Allergenic Extract [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class PE:	Increased Histamine Release [PE] Cell-mediated Immunity [PE] Increased IgG Production [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:	Allergens [CS] Plant Proteins [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:	Allergens [CS] Cell-mediated Immunity [PE] Increased Histamine Release [PE] Standardized Chemical Allergen [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
62106-1147-8	1 BOTTLE, GLASS in 1 CARTON (62106-1147-8) / 20 mL in 1 BOTTLE, GLASS	08 May, 2015	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

Unda 48

Condurango & more..

Liquid
Seroyal USA
NDC: 62106-1147

Purpose:

Uses for the temporary relief of symptoms associated with abdominal cramping, bloating and gas following meals.

Uses for the temporary relief of symptoms associated with difficult urination and occasional incontinence.

Indications to help with calcium absorption and for symptoms associated with minor respiratory problems.

Uses for the temporary relief of symptoms associated with minor urinary discomfort.

Uses for the temporary relief of minor symptoms associated with low energy and fatigue.

Product Elements:

Unda 16 saxifraga granulata, origanum vulgare, lactuca virosa, veronica officinalis, ajuga reptans, drosera, senega officinalis, aurum metallicum, argentum metallicum veronica officinalis flowering top veronica officinalis flowering top ajuga reptans whole ajuga reptans whole drosera rotundifolia flowering top drosera rotundifolia flowering top polygala senega root polygala senega root gold gold saxifraga granulata whole saxifraga granulata whole origanum vulgare subsp. hirtum whole origanum vulgare subsp. hirtum whole alcohol lactuca virosa lactuca virosa silver silver water unda 3 equisetum arvense stem, chamomilla, condurango bark, viola tricolor, boldo leaf, aluminium metallicum, stannum metallicum equisetum arvense top equisetum arvense top matricaria recutita matricaria recutita marsdenia condurango bark marsdenia condurango bark viola tricolor viola tricolor peumus boldus leaf peumus boldus leaf water aluminum aluminum alcohol tin tin unda 48 condurango, calendula officinalis, lycopodium clavatum, sabina, thuja occidentalis, aurum metallicum, plumbum metallicum, arsenicum album marsdenia condurango bark marsdenia condurango bark calendula officinalis flowering top calendula officinalis flowering top water lycopodium clavatum spore lycopodium clavatum spore juniperus sabina leaf juniperus sabina leaf thuja occidentalis leafy twig thuja occidentalis leafy twig gold gold lead lead arsenic trioxide arsenic cation (3+) alcohol unda 7 equisetum arvense, uva-ursi, juniperus communis, cytisus scoparius, hieraciumpilosella, argentum metallicum hieracium pilosella whole hieracium pilosella whole alcohol equisetum arvense top equisetum arvense top arctostaphylos uva-ursi leaf arctostaphylos uva-ursi leaf juniperus communis whole juniperus communis whole cytisus scoparius flowering top cytisus scoparius flowering top silver silver water unda 45 equisetum arvense, millefolium, saxifraga granulata, dulcamara, uva-ursi, argentum metallicum, stannum metallicum saxifraga granulata whole saxifraga granulata whole equisetum arvense top equisetum arvense top achillea millefolium achillea millefolium solanum dulcamara top solanum dulcamara top arctostaphylos uva-ursi leaf arctostaphylos uva-ursi leaf tin tin alcohol water silver silver

Indications and Usage:

Uses for the temporary relief of symptoms associated with abdominal cramping, bloating and gas following meals. directions adults and adolescents (12 years and older) take 5 drops three times daily or as recommended by your healthcare practitioner. children (under 12 years) take under the direction of your healthcare practitioner.

Uses for the temporary relief of symptoms associated with difficult urination and occasional incontinence. directions adults and adolescents (12 years and older) take 5 drops three times daily or as recommended by your healthcare practitioner. children (under 12 years) take under the direction of your healthcare practitioner.

Indications to help with calcium absorption and for symptoms associated with minor respiratory problems. directions adults and adolescents (12 years and older) take 5 drops three times daily or as recommended by your healthcare practitioner. children (under 12 years) take under the direction of your healthcare practitioner.

Uses for the temporary relief of symptoms associated with minor urinary discomfort. directions adults and adolescents (12 years and older) take 5 drops three times daily or as recommended by your healthcare practitioner. children (under 12 years) take under the direction of your healthcare practitioner.

Uses for the temporary relief of minor symptoms associated with low energy and fatigue. directions adults and adolescents (12 years and older) take 5 drops three times daily or as recommended by your healthcare practitioner children (under 12 years) take under the direction of your healthcare practitioner.

Warnings:

Warnings stop use and ask a doctor if symptoms persist or worsen. if pregnant or breastfeeding, ask a health professional before use. keep out of reach of children. in case of overdose, get medical help or contact a poison control center right away.

Warnings if pregnant or breastfeeding, ask a health professional before use. keep out of reach of children. in case of overdose, get medical help or contact a poison control center right away. if symptoms persist or worsen, consult your healthcare practitioner.

Dosage and Administration:

Directions adults and adolescents (12 years and older) take 5 drops three times daily or as recommended by your healthcare practitioner. children (under 12 years) take under the direction of your healthcare practitioner.

Overdosage:

In case of overdose,get medical help or contact a poison control center right away.

In case of overdose, get medical help or contact a poison control center right away.

Package Label Principal Display Panel:

Ndc 62106-1102-8 unda numbered compounds unda 3 homeopathic preparation for the temporary relief of symptoms associated with abdominal cramping, bloating and gas following meals. contains 31% alcohol 0.7 fl oz (20 ml) 62106-1102

Ndc 62106-1106-8 unda numbered compounds unda 7 homeopathic preparation for the temporary relief of symptoms associated with difficult urination and occasional incontinence. contains 31% alcohol 0.7 fl oz (20 ml) 62106-1106-8

Unda numbered compounds ndc 62106-1115-8 unda 16 homeopathic preparation for the temporary relief of symptoms associated with minor respiratory problems. contains 31% alcohol 0.7 fl oz (20 ml) 62106-1115

Ndc 62106-1144-8 unda numbered compounds unda 45 homeopathic preparation for the temporary relief of symptoms associated with minor urinary discomfort. contains 31% alcohol 0.7 fl oz (20 ml) 62106-1144-8

Ndc 62106-1147-8 unda numbered compounds unda 48 homeopathic preparation for the temporary relief of minor symptoms associated with low energy and fatigue. contains 31% alcohol 0.7 fl oz (20 ml) 62106-1147

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.