Hptp

Arnica Montana, Achillea Millefolium, Erigeron Canadensis, Hydrastis Canadensis, Oryctolagus Cuniculus, Sabina, Secale Cornutum

Seroyal Usa
Human Otc Drug
NDC 62106-0630

Hptp also known as Arnica Montana, Achillea Millefolium, Erigeron Canadensis, Hydrastis Canadensis, Oryctolagus Cuniculus, Sabina, Secale Cornutum is a human otc drug labeled by 'Seroyal Usa'. National Drug Code (NDC) number for Hptp is 62106-0630. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Hptp drug includes Achillea Millefolium - 6 [hp_X]/30mL Arnica Montana Root - 6 [hp_X]/30mL Claviceps Purpurea Sclerotium - 8 [hp_X]/30mL Conyza Canadensis - 6 [hp_X]/30mL Goldenseal - 6 [hp_X]/30mL Juniperus Sabina Leafy Twig - 8 [hp_X]/30mL Oryctolagus Cuniculus Adrenal Gland - 10 [hp_X]/30mL Oryctolagus Cuniculus Pituitary Gland - 10 [hp_X]/30mL . The currest status of Hptp drug is Active.

Drug Information:

Drug NDC:	62106-0630
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:	Hptp
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:	Arnica Montana, Achillea Millefolium, Erigeron Canadensis, Hydrastis Canadensis, Oryctolagus Cuniculus, Sabina, Secale Cornutum
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:	ACHILLEA MILLEFOLIUM - 6 [hp_X]/30mL ARNICA MONTANA ROOT - 6 [hp_X]/30mL CLAVICEPS PURPUREA SCLEROTIUM - 8 [hp_X]/30mL CONYZA CANADENSIS - 6 [hp_X]/30mL GOLDENSEAL - 6 [hp_X]/30mL JUNIPERUS SABINA LEAFY TWIG - 8 [hp_X]/30mL ORYCTOLAGUS CUNICULUS ADRENAL GLAND - 10 [hp_X]/30mL ORYCTOLAGUS CUNICULUS PITUITARY GLAND - 10 [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:	26 Oct, 2015
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	13 Jun, 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.
UPC:	0883196138203
UPC stands for Universal Product Code.
UNII:	2FXJ6SW4PK MUE8Y11327 01G9XEA93N ZW3Z11D0JV Z5BEX9K2G1 QGY289M89Q T9F9ZW799A
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
62106-0630-0	1 BOTTLE, GLASS in 1 CARTON (62106-0630-0) / 30 mL in 1 BOTTLE, GLASS	26 Oct, 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

Hptp

Arnica Montana & more..

Liquid
Seroyal USA
NDC: 62106-0630

Purpose:

Uses helps promote and maintain growth and development normal energy levels

Product Elements:

Hptp arnica montana, achillea millefolium, erigeron canadensis, hydrastis canadensis, oryctolagus cuniculus, sabina, secale cornutum juniperus sabina leafy twig juniperus sabina leafy twig claviceps purpurea sclerotium claviceps purpurea sclerotium arnica montana root arnica montana root achillea millefolium achillea millefolium conyza canadensis conyza canadensis goldenseal goldenseal oryctolagus cuniculus pituitary gland oryctolagus cuniculus pituitary gland alcohol water oryctolagus cuniculus adrenal gland oryctolagus cuniculus adrenal gland

Indications and Usage:

Uses helps promote and maintain growth and development normal energy levels. 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.

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 62106-0630-0 hptp homeopathic preparation to help promote and maintain growth and development. contains 31% alcohol 1 fl oz (30 ml) 62106-0630-0

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.