Acidum Phosphoricum Plex

Anacardium Orientale, Argentum Nitricum, Arnica Montana, Avena Sativa, Gelsemium Sempervirens, Kali Phosphoricum, Phosphoricum Acidum, Selenium Metallicum

Seroyal Usa
Human Otc Drug
NDC 62106-1205

Acidum Phosphoricum Plex also known as Anacardium Orientale, Argentum Nitricum, Arnica Montana, Avena Sativa, Gelsemium Sempervirens, Kali Phosphoricum, Phosphoricum Acidum, Selenium Metallicum is a human otc drug labeled by 'Seroyal Usa'. National Drug Code (NDC) number for Acidum Phosphoricum Plex is 62106-1205. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Acidum Phosphoricum Plex drug includes Arnica Montana Root - 6 [hp_X]/30mL Avena Sativa Flowering Top - 3 [hp_X]/30mL Gelsemium Sempervirens Root - 6 [hp_X]/30mL Phosphoric Acid - 6 [hp_X]/30mL Potassium Phosphate, Dibasic - 6 [hp_X]/30mL Selenium - 6 [hp_X]/30mL Semecarpus Anacardium Juice - 6 [hp_X]/30mL Silver Nitrate - 6 [hp_X]/30mL . The currest status of Acidum Phosphoricum Plex drug is Active.

Drug Information:

Drug NDC:	62106-1205
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:	Acidum Phosphoricum Plex
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:	Anacardium Orientale, Argentum Nitricum, Arnica Montana, Avena Sativa, Gelsemium Sempervirens, Kali Phosphoricum, Phosphoricum Acidum, Selenium Metallicum
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:	ARNICA MONTANA ROOT - 6 [hp_X]/30mL AVENA SATIVA FLOWERING TOP - 3 [hp_X]/30mL GELSEMIUM SEMPERVIRENS ROOT - 6 [hp_X]/30mL PHOSPHORIC ACID - 6 [hp_X]/30mL POTASSIUM PHOSPHATE, DIBASIC - 6 [hp_X]/30mL SELENIUM - 6 [hp_X]/30mL SEMECARPUS ANACARDIUM JUICE - 6 [hp_X]/30mL SILVER NITRATE - 6 [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:	15 Dec, 2015
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	10 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, 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.
UNII:	MUE8Y11327 MA9CQJ3F7F 639KR60Q1Q E4GA8884NN CI71S98N1Z H6241UJ22B Y0F0BU8RDU 95IT3W8JZE
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.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
62106-1205-0	1 BOTTLE, GLASS in 1 CARTON (62106-1205-0) / 30 mL in 1 BOTTLE, GLASS	15 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

Acidum Phosphoricum Plex

Anacardium Orientale & more..

Liquid
Seroyal USA
NDC: 62106-1205

Purpose:

Uses helps promote and support overall nervous system health. assists with the temporary relief of symptoms associated with mental fatigue.

Product Elements:

Acidum phosphoricum plex anacardium orientale, argentum nitricum, arnica montana, avena sativa, gelsemium sempervirens, kali phosphoricum, phosphoricum acidum, selenium metallicum silver nitrate silver cation arnica montana root arnica montana root avena sativa flowering top avena sativa flowering top potassium phosphate, dibasic phosphate ion selenium selenium alcohol water semecarpus anacardium juice semecarpus anacardium juice gelsemium sempervirens root gelsemium sempervirens root phosphoric acid phosphoric acid

Indications and Usage:

Uses helps promote and support overall nervous system health. assists with the temporary relief of symptoms associated with mental fatigue. directions to be taken ten minutes away from food. invert bottle and shake lightly allowing drops to fall directly under the tongue or into Â¼ oz of water. hold contents for about 20 seconds and swallow. to promote drop flow, invert bottle and shake before each use. dosage frequency may be increased up to six times daily depending on the severity of symptoms. adults and adolescents (12 years and older) take 10 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.

Dosage and Administration:

Directions to be taken ten minutes away from food. invert bottle and shake lightly allowing drops to fall directly under the tongue or into Â¼ oz of water. hold contents for about 20 seconds and swallow. to promote drop flow, invert bottle and shake before each use. dosage frequency may be increased up to six times daily depending on the severity of symptoms. adults and adolescents (12 years and older) take 10 drops 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:

Ndc 62106-1205-0 unda plex acidum phosphoricum plex homeopathic preparation for the temporary relief of mental fatigue symptoms. contains 60% alcohol 1 fl oz (30 ml) 62106-1205

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.