Damiana Complex

Agnes Castus, Avena Sativa, Damiana, Gelsemium Sempervirens, Ignatia Amara, Lycopodium Clavatum, Orchitinum, Phosphoricum Acidum, Sabal Serrulata, Selenium Metallicum.

Ohm Pharma Inc.
Human Otc Drug
NDC 66096-726

Damiana Complex also known as Agnes Castus, Avena Sativa, Damiana, Gelsemium Sempervirens, Ignatia Amara, Lycopodium Clavatum, Orchitinum, Phosphoricum Acidum, Sabal Serrulata, Selenium Metallicum. is a human otc drug labeled by 'Ohm Pharma Inc.'. National Drug Code (NDC) number for Damiana Complex is 66096-726. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Damiana Complex drug includes Avena Sativa Flowering Top - 3 [hp_X]/59mL Chaste Tree - 3 [hp_X]/59mL Gelsemium Sempervirens Root - 12 [hp_X]/59mL Lycopodium Clavatum Spore - 12 [hp_X]/59mL Phosphoric Acid - 12 [hp_X]/59mL Saw Palmetto - 3 [hp_X]/59mL Selenium - 12 [hp_X]/59mL Strychnos Ignatii Seed - 12 [hp_X]/59mL Sus Scrofa Testicle - 12 [hp_X]/59mL Turnera Diffusa Leafy Twig - 3 [hp_X]/59mL . The currest status of Damiana Complex drug is Active.

Drug Information:

Drug NDC:	66096-726
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:	Damiana Complex
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:	Agnes Castus, Avena Sativa, Damiana, Gelsemium Sempervirens, Ignatia Amara, Lycopodium Clavatum, Orchitinum, Phosphoricum Acidum, Sabal Serrulata, Selenium Metallicum.
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Ohm Pharma Inc.
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:	AVENA SATIVA FLOWERING TOP - 3 [hp_X]/59mL CHASTE TREE - 3 [hp_X]/59mL GELSEMIUM SEMPERVIRENS ROOT - 12 [hp_X]/59mL LYCOPODIUM CLAVATUM SPORE - 12 [hp_X]/59mL PHOSPHORIC ACID - 12 [hp_X]/59mL SAW PALMETTO - 3 [hp_X]/59mL SELENIUM - 12 [hp_X]/59mL STRYCHNOS IGNATII SEED - 12 [hp_X]/59mL SUS SCROFA TESTICLE - 12 [hp_X]/59mL TURNERA DIFFUSA LEAFY TWIG - 3 [hp_X]/59mL
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:	19 Aug, 2015
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	16 Jan, 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:	OHM PHARMA INC.
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:	0366096726058
UPC stands for Universal Product Code.
UNII:	MA9CQJ3F7F 433OSF3U8A 639KR60Q1Q C88X29Y479 E4GA8884NN J7WWH9M8QS H6241UJ22B 1NM3M2487K KM02613O28 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
66096-726-05	59 mL in 1 BOTTLE, SPRAY (66096-726-05)	19 Aug, 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

Damiana Complex

Agnes Castus & more..

Liquid
OHM PHARMA INC.
NDC: 66096-726

Purpose:

Temporarily relieves low stamina.

Product Elements:

Damiana complex agnes castus, avena sativa, damiana, gelsemium sempervirens, ignatia amara, lycopodium clavatum, orchitinum, phosphoricum acidum, sabal serrulata, selenium metallicum. alcohol glycerin water chaste tree chaste tree avena sativa flowering top avena sativa flowering top turnera diffusa leafy twig turnera diffusa leafy twig gelsemium sempervirens root gelsemium sempervirens root strychnos ignatii seed strychnos ignatii seed lycopodium clavatum spore lycopodium clavatum spore sus scrofa testicle sus scrofa testicle phosphoric acid phosphoric acid saw palmetto saw palmetto selenium selenium

Indications and Usage:

Uses: temporarily relieves low stamina.** ** ?claims based on traditional homepathic practice, not accepted medical evidence. not fda evaluated.

Warnings:

Warnings: if pregnant or breast- feeding, ask a health professional before use. if symptoms worsen or persist for more than a week, discontinue use and contact a doctor. ?keep out of reach of children.

Dosage and Administration:

Directions: shake 10 times before use. adults: spray 3 times under the tongue 2-3 times a day or as directed by a health care professional. not for use by children.

Package Label Principal Display Panel:

Homeopathic medicine ndc: 66096-726-05 damiana complex natural - safe - effective no side effects 2 fl oz (59 ml) / 15% alcohol product of usa 2oz bottle label temporarily relieves low stamina.

Further Questions:

Mfg. by: ohm pharma, inc. mineral wells, tx 76067 www.ohmpharma.com

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.