Guna-male

Adenosinum Ciclophosphoricum - Melatonin - Phosphorus - Sus Scrofa Adrenal Gland - Sus Scrofa Hypothalamus - Sus Scrofa Pancreas - Sus Scrofa Pineal Gland - Sus Scrofa Pituitary Gland - Sus Scrofa Testicle - Sus Scrofa Thymus - Thyroid - Turnera Diffusa Top -

Guna Spa
Human Otc Drug
NDC 17089-233

Guna-male also known as Adenosinum Ciclophosphoricum - Melatonin - Phosphorus - Sus Scrofa Adrenal Gland - Sus Scrofa Hypothalamus - Sus Scrofa Pancreas - Sus Scrofa Pineal Gland - Sus Scrofa Pituitary Gland - Sus Scrofa Testicle - Sus Scrofa Thymus - Thyroid - Turnera Diffusa Top - is a human otc drug labeled by 'Guna Spa'. National Drug Code (NDC) number for Guna-male is 17089-233. This drug is available in dosage form of Solution/ Drops. The names of the active, medicinal ingredients in Guna-male drug includes Adenosine Cyclic Phosphate - 6 [hp_X]/30mL Melatonin - 30 [hp_X]/30mL Phosphorus - 6 [hp_X]/30mL Sus Scrofa Adrenal Gland - 30 [hp_X]/30mL Sus Scrofa Hypothalamus - 30 [hp_X]/30mL Sus Scrofa Pancreas - 30 [hp_X]/30mL Sus Scrofa Pineal Gland - 30 [hp_X]/30mL Sus Scrofa Pituitary Gland - 30 [hp_X]/30mL Sus Scrofa Testicle - 30 [hp_X]/30mL Sus Scrofa Thymus - 30 [hp_X]/30mL and more. The currest status of Guna-male drug is Active.

Drug Information:

Drug NDC:	17089-233
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:	Guna-male
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:	Adenosinum Ciclophosphoricum - Melatonin - Phosphorus - Sus Scrofa Adrenal Gland - Sus Scrofa Hypothalamus - Sus Scrofa Pancreas - Sus Scrofa Pineal Gland - Sus Scrofa Pituitary Gland - Sus Scrofa Testicle - Sus Scrofa Thymus - Thyroid - Turnera Diffusa Top -
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Guna Spa
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Solution/ Drops
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:	ADENOSINE CYCLIC PHOSPHATE - 6 [hp_X]/30mL MELATONIN - 30 [hp_X]/30mL PHOSPHORUS - 6 [hp_X]/30mL SUS SCROFA ADRENAL GLAND - 30 [hp_X]/30mL SUS SCROFA HYPOTHALAMUS - 30 [hp_X]/30mL SUS SCROFA PANCREAS - 30 [hp_X]/30mL SUS SCROFA PINEAL GLAND - 30 [hp_X]/30mL SUS SCROFA PITUITARY GLAND - 30 [hp_X]/30mL SUS SCROFA TESTICLE - 30 [hp_X]/30mL SUS SCROFA THYMUS - 30 [hp_X]/30mL Load more... THYROID - 30 [hp_X]/30mL TURNERA DIFFUSA LEAFY TWIG - 6 [hp_X]/30mL
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:	23 May, 2006
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	22 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:	Guna spa
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:	0317089233183
UPC stands for Universal Product Code.
UNII:	E0399OZS9N JL5DK93RCL 27YLU75U4W 398IYQ16YV N6R0856Z79 9Y3J3362RY 050QZ2EDK7 L0PFEMQ1DT KM02613O28 7B69B0BD62 Load more... 0B4FDL9I6P RQ2CFA7WWJ
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
17089-233-18	1 BOTTLE, DROPPER in 1 BOX (17089-233-18) / 30 mL in 1 BOTTLE, DROPPER	21 Dec, 2018	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

Guna-male

Adenosinum Ciclophosphoricum - Melatonin - Phosphorus - Sus Scrofa Adrenal Gland - Sus Scrofa Hypothalamus - Sus Scrofa Pancreas - Sus Scrofa Pineal Gland - Sus Scrofa Pituitary Gland - Sus Scrofa Testicle - Sus Scrofa Thymus - Thyroid - Turnera Diffusa Top - & more..

Solution/ Drops
Guna spa
NDC: 17089-233

Purpose:

Uses temporary relief of symptoms due to hormonal imbalances, such as: mood fluctuations irritability sleep disturbance

Product Elements:

Guna-male adenosinum ciclophosphoricum - melatonin - phosphorus - sus scrofa adrenal gland - sus scrofa hypothalamus - sus scrofa pancreas - sus scrofa pineal gland - sus scrofa pituitary gland - sus scrofa testicle - sus scrofa thymus - thyroid - turnera diffusa top - alcohol adenosine cyclic phosphate adenosine cyclic phosphate turnera diffusa leafy twig turnera diffusa leafy twig sus scrofa adrenal gland sus scrofa adrenal gland sus scrofa pituitary gland sus scrofa pituitary gland sus scrofa hypothalamus sus scrofa hypothalamus melatonin melatonin sus scrofa testicle sus scrofa testicle sus scrofa pancreas sus scrofa pancreas phosphorus phosphorus sus scrofa pineal gland sus scrofa pineal gland sus scrofa thymus sus scrofa thymus thyroid thyroid

Indications and Usage:

Take 15 minutes before meals.

Warnings:

Warnings stop use and ask doctor if symptoms persist more than 5 days. if pregnant or breast-feeding 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 ethyl alcohol 30%

Dosage and Administration:

Directions take 15 minutes before meals adults and children 12 years and older 20 drops in a little water 2 times per day children between 12 years and 6 years of age ask your doctor. children under 9 years ask your doctor.

Package Label Principal Display Panel:

Principal display panel 5usk2m-rev06-25-05-18

Further Questions:

Questions questions?: info@gunainc.com tel. (484) 223-3500

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.