Hki

Atropinum Sulphuricum, Benzoicum Acidum, Berberis Vulgaris, Calcarea Carbonica, Colocynthis, Coccus Cacti, Lapis Albus, Lithium Carbonicum, Lycopodium Clavatum, Oryctolagus Cuniculus Kidney, Rubia Tinctorum, Sarsaparilla, Urtica Urens

Seroyal Usa
Human Otc Drug
NDC 62106-0625

Hki also known as Atropinum Sulphuricum, Benzoicum Acidum, Berberis Vulgaris, Calcarea Carbonica, Colocynthis, Coccus Cacti, Lapis Albus, Lithium Carbonicum, Lycopodium Clavatum, Oryctolagus Cuniculus Kidney, Rubia Tinctorum, Sarsaparilla, Urtica Urens is a human otc drug labeled by 'Seroyal Usa'. National Drug Code (NDC) number for Hki is 62106-0625. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Hki drug includes Atropine Sulfate - 6 [hp_X]/30mL Benzoic Acid - 6 [hp_X]/30mL Berberis Vulgaris Root Bark - 5 [hp_X]/30mL Calcium Hexafluorosilicate - 12 [hp_C]/30mL Citrullus Colocynthis Fruit Pulp - 6 [hp_X]/30mL Lithium Carbonate - 6 [hp_X]/30mL Lycopodium Clavatum Spore - 5 [hp_X]/30mL Oryctolagus Cuniculus Kidney - 10 [hp_X]/30mL Oyster Shell Calcium Carbonate, Crude - 12 [hp_X]/30mL Protortonia Cacti - 5 [hp_X]/30mL and more. The currest status of Hki drug is Active.

Drug Information:

Drug NDC:	62106-0625
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:	Hki
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:	Atropinum Sulphuricum, Benzoicum Acidum, Berberis Vulgaris, Calcarea Carbonica, Colocynthis, Coccus Cacti, Lapis Albus, Lithium Carbonicum, Lycopodium Clavatum, Oryctolagus Cuniculus Kidney, Rubia Tinctorum, Sarsaparilla, Urtica Urens
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:	ATROPINE SULFATE - 6 [hp_X]/30mL BENZOIC ACID - 6 [hp_X]/30mL BERBERIS VULGARIS ROOT BARK - 5 [hp_X]/30mL CALCIUM HEXAFLUOROSILICATE - 12 [hp_C]/30mL CITRULLUS COLOCYNTHIS FRUIT PULP - 6 [hp_X]/30mL LITHIUM CARBONATE - 6 [hp_X]/30mL LYCOPODIUM CLAVATUM SPORE - 5 [hp_X]/30mL ORYCTOLAGUS CUNICULUS KIDNEY - 10 [hp_X]/30mL OYSTER SHELL CALCIUM CARBONATE, CRUDE - 12 [hp_X]/30mL PROTORTONIA CACTI - 5 [hp_X]/30mL Load more... RUBIA TINCTORUM ROOT - 4 [hp_X]/30mL SARSAPARILLA - 1 [hp_X]/30mL URTICA URENS - 1 [hp_X]/30mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	SUBLINGUAL
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:	14 Dec, 2015
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	09 May, 2026
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, 2024
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:	0883196138500
UPC stands for Universal Product Code.
NUI:	N0000175806 N0000175807
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	03J5ZE7KA5 8SKN0B0MIM 1TH8Q20J0U 2NVP93XVQ3 23H32AOH17 2BMD2GNA4V C88X29Y479 482QQ7H44Q 2E32821G6I LZB7TFX1LT Load more... 0SVP95L23G 2H1576D5WG IHN2NQ5OF9
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 MOA:	Ammonium Ion Binding Activity [MoA]
Mechanism of action of the drug—molecular, subcellular, or cellular functional activity—of the drug’s established pharmacologic class. Takes the form of the mechanism of action, followed by `[MoA]` (such as `Calcium Channel Antagonists [MoA]` or `Tumor Necrosis Factor Receptor Blocking Activity [MoA]`.
Pharmacologic Class EPC:	Nitrogen Binding Agent [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:	Ammonium Ion Binding Activity [MoA] Anticholinergic [EPC] Cholinergic Antagonists [MoA] Cholinergic Muscarinic Antagonist [EPC] Cholinergic Muscarinic Antagonists [MoA] Mood Stabilizer [EPC] Nitrogen Binding Agent [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
62106-0625-0	1 BOTTLE, GLASS in 1 CARTON (62106-0625-0) / 30 mL in 1 BOTTLE, GLASS	14 Dec, 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

Hki

Atropinum Sulphuricum & more..

Liquid
Seroyal USA
NDC: 62106-0625

Purpose:

Uses helps promote and maintain healthy kidney and urinary tract functions.

Product Elements:

Hki atropinum sulphuricum, benzoicum acidum, berberis vulgaris, calcarea carbonica, colocynthis, coccus cacti, lapis albus, lithium carbonicum, lycopodium clavatum, oryctolagus cuniculus kidney, rubia tinctorum, sarsaparilla, urtica urens atropine sulfate atropine oyster shell calcium carbonate, crude oyster shell calcium carbonate, crude citrullus colocynthis fruit pulp citrullus colocynthis fruit pulp lycopodium clavatum spore lycopodium clavatum spore oryctolagus cuniculus kidney oryctolagus cuniculus kidney sarsaparilla sarsaparilla calcium hexafluorosilicate calcium hexafluorosilicate benzoic acid benzoic acid protortonia cacti protortonia cacti lithium carbonate lithium cation alcohol rubia tinctorum root rubia tinctorum root urtica urens urtica urens water berberis vulgaris root bark berberis vulgaris root bark

Indications and Usage:

Uses helps promote and maintain healthy kidney and urinary tract functions. directions to be taken 20 minutes away from food. place drops directly under the tongue or into Â¼ oz of water. adults and adolescents (12 years and older): take 10 drops two to 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. contains shellfish (oyster)

Do Not Use:

Dosage and Administration:

Directions to be taken 20 minutes away from food. place drops directly under the tongue or into Â¼ oz of water. adults and adolescents (12 years and older): take 10 drops two to three times daily or as recommended by your healthcare practitioner. children (under 12 years): take under the direction of your healthcare practitioner.

Stop Use:

Stop use and ask a doctor if symptoms persist or worsen.

Overdosage:

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

Package Label Principal Display Panel:

Genestra brands ndc 62106-0625-0 hki homeopathic preparation to help promote and maintain kidney and urinary tract health. contains 48% alcohol 1 fl oz (30 ml) hki pdp hki warnings

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.