Female Support

Chamomilla, Cimicifuga Racemosa, Helonias Dioica, Mentha Piperita, Senna (cassia Angustifolia), Valeriana Officinalis, Viola Odorata, Agnus Castus, Ledum Palustre, Lilium Tigrinum, Staphysagria, Crocus Sativus, Hydrastis Canadensis, Cinchona Officinalis, Convallaria Majalis, Cyclamen Europaeum, Cinnamomum, Murex Purpurea, Naja Tripudians

Deseret Biologicals, Inc.
Human Prescription Drug
NDC 43742-1629

Female Support also known as Chamomilla, Cimicifuga Racemosa, Helonias Dioica, Mentha Piperita, Senna (cassia Angustifolia), Valeriana Officinalis, Viola Odorata, Agnus Castus, Ledum Palustre, Lilium Tigrinum, Staphysagria, Crocus Sativus, Hydrastis Canadensis, Cinchona Officinalis, Convallaria Majalis, Cyclamen Europaeum, Cinnamomum, Murex Purpurea, Naja Tripudians is a human prescription drug labeled by 'Deseret Biologicals, Inc.'. National Drug Code (NDC) number for Female Support is 43742-1629. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Female Support drug includes Black Cohosh - 3 [hp_X]/mL Chamaelirium Luteum Root - 3 [hp_X]/mL Chaste Tree Fruit - 4 [hp_X]/mL Cinchona Officinalis Bark - 8 [hp_X]/mL Cinnamon - 12 [hp_X]/mL Convallaria Majalis - 8 [hp_X]/mL Cyclamen Purpurascens Tuber - 8 [hp_X]/mL Delphinium Staphisagria Seed - 4 [hp_X]/mL Goldenseal - 6 [hp_X]/mL Hexaplex Trunculus Hypobranchial Gland Juice - 12 [hp_X]/mL and more. The currest status of Female Support drug is Active.

Drug Information:

Drug NDC:	43742-1629
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:	Female Support
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Prescription 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:	Chamomilla, Cimicifuga Racemosa, Helonias Dioica, Mentha Piperita, Senna (cassia Angustifolia), Valeriana Officinalis, Viola Odorata, Agnus Castus, Ledum Palustre, Lilium Tigrinum, Staphysagria, Crocus Sativus, Hydrastis Canadensis, Cinchona Officinalis, Convallaria Majalis, Cyclamen Europaeum, Cinnamomum, Murex Purpurea, Naja Tripudians
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Deseret Biologicals, 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:	BLACK COHOSH - 3 [hp_X]/mL CHAMAELIRIUM LUTEUM ROOT - 3 [hp_X]/mL CHASTE TREE FRUIT - 4 [hp_X]/mL CINCHONA OFFICINALIS BARK - 8 [hp_X]/mL CINNAMON - 12 [hp_X]/mL CONVALLARIA MAJALIS - 8 [hp_X]/mL CYCLAMEN PURPURASCENS TUBER - 8 [hp_X]/mL DELPHINIUM STAPHISAGRIA SEED - 4 [hp_X]/mL GOLDENSEAL - 6 [hp_X]/mL HEXAPLEX TRUNCULUS HYPOBRANCHIAL GLAND JUICE - 12 [hp_X]/mL Load more... LEDUM PALUSTRE TWIG - 4 [hp_X]/mL LILIUM LANCIFOLIUM WHOLE FLOWERING - 4 [hp_X]/mL MATRICARIA RECUTITA - 3 [hp_X]/mL MENTHA PIPERITA - 3 [hp_X]/mL NAJA NAJA VENOM - 15 [hp_X]/mL SAFFRON - 6 [hp_X]/mL SENNA LEAF - 3 [hp_X]/mL VALERIAN - 3 [hp_X]/mL VIOLA ODORATA - 3 [hp_X]/mL
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:	18 Mar, 2020
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	22 Apr, 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:	23 Dec, 2025
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:	Deseret Biologicals, 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.
NUI:	N0000185371 N0000175629 N0000184306 M0006342 M0008672 M0000728
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	K73E24S6X9 DQV54Y5H3U 433OSF3U8A S003A158SB 5S29HWU6QB QHH4HVF5QE G728143D8Q 00543AP1JV ZW3Z11D0JV IQV54TN60Y Load more... 877L01IZ0P X67Z2963PI G0R4UBI2ZZ 79M2M2UDA9 ZZ4AG7L7VM E849G4X5YJ AK7JF626KX JWF5YAW3QW AET12U8B74
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 EPC:	Non-Standardized Food Allergenic Extract [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 PE:	Increased Histamine Release [PE] Cell-mediated Immunity [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:	Dietary Proteins [CS] Food Additives [CS] Allergens [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:	Allergens [CS] Cell-mediated Immunity [PE] Dietary Proteins [CS] Food Additives [CS] Increased Histamine Release [PE] Non-Standardized Food Allergenic Extract [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
43742-1629-1	30 mL in 1 BOTTLE, DROPPER (43742-1629-1)	18 Mar, 2020	22 Apr, 2026	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

Female Support

Chamomilla & more..

Liquid
Deseret Biologicals, Inc.
NDC: 43742-1629

Purpose:

Homeopathic indications: for temporary relief of symptoms related to hormonal dysfunction including fluid retention, hot flashes, painful menses, irregular and painful menstruation, and mood swings.** ** these statements are based upon homeopathic principles. they have not been reviewed by the food and drug administration.

Product Elements:

Female support chamomilla, cimicifuga racemosa, helonias dioica, mentha piperita, senna (cassia angustifolia), valeriana officinalis, viola odorata, agnus castus, ledum palustre, lilium tigrinum, staphysagria, crocus sativus, hydrastis canadensis, cinchona officinalis, convallaria majalis, cyclamen europaeum, cinnamomum, murex purpurea, naja tripudians matricaria recutita matricaria chamomilla black cohosh black cohosh chamaelirium luteum root chamaelirium luteum root mentha piperita mentha piperita senna leaf senna leaf valerian valerian viola odorata viola odorata chaste tree fruit chaste tree ledum palustre twig ledum palustre twig lilium lancifolium whole flowering lilium lancifolium whole flowering delphinium staphisagria seed delphinium staphisagria seed saffron saffron goldenseal goldenseal cinchona officinalis bark cinchona officinalis bark convallaria majalis convallaria majalis cyclamen purpurascens tuber cyclamen purpurascens tuber cinnamon cinnamon hexaplex trunculus hypobranchial gland juice hexaplex trunculus hypobranchial gland juice naja naja venom naja naja venom water alcohol

Indications and Usage:

Warnings:

Warnings: keep out of reach of children. in case of overdose, contact a physician or poison control center right away. if pregnant or breast-feeding, ask a health professional before use. tamper seal: "sealed for your protection." do not use if seal is broken or missing.

Dosage and Administration:

Directions: 1-10 drops under the tongue, 3 times a day or as directed by a health professional. consult a physician for use in children under 12 years of age.

Package Label Principal Display Panel:

Package label display: des bio ndc 43742-1629-1 homeopathic female support 1 fl oz (30ml) female support

Further Questions:

Questions: dist. by: deseret biologicals, inc. 469 w. parkland drive sandy, ut 84070 www.desbio.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.