Female Stimulant

Lilium Tigrinum, Bovista, Cypripedium Pubescens, Hydrastis Canadensis, Petroselinum Sativum, Aquilegia Vulgaris, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Heart (suis), Kreosotum, Oophorinum (suis), Uterus (suis), Folliculinum, Lachesis Mutus, Magnesia Phosphorica, Mercurius Solubilis, Sepia, Pineal Gland (suis), Hypophysis Suis, Aconiticum Acidum Cis-, Apis Venenum Purum, Estradiol, Progesterone, Testosterone, Placenta Totalis Suis, Faecalis (alkaligenes), Mutabile Bacillus (bach)


Deseret Biologicals, Inc.
Human Otc Drug
NDC 43742-1507
Female Stimulant also known as Lilium Tigrinum, Bovista, Cypripedium Pubescens, Hydrastis Canadensis, Petroselinum Sativum, Aquilegia Vulgaris, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Heart (suis), Kreosotum, Oophorinum (suis), Uterus (suis), Folliculinum, Lachesis Mutus, Magnesia Phosphorica, Mercurius Solubilis, Sepia, Pineal Gland (suis), Hypophysis Suis, Aconiticum Acidum Cis-, Apis Venenum Purum, Estradiol, Progesterone, Testosterone, Placenta Totalis Suis, Faecalis (alkaligenes), Mutabile Bacillus (bach) is a human otc drug labeled by 'Deseret Biologicals, Inc.'. National Drug Code (NDC) number for Female Stimulant is 43742-1507. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Female Stimulant drug includes Aconitic Acid, (z)- - 10 [hp_X]/mL Alcaligenes Faecalis - 30 [hp_C]/mL Apis Mellifera Venom - 18 [hp_X]/mL Aquilegia Vulgaris - 8 [hp_X]/mL Cypripedium Parviflorum Var. Pubescens Root - 6 [hp_X]/mL Escherichia Coli - 30 [hp_C]/mL Estradiol - 30 [hp_X]/mL Estrone - 8 [hp_X]/mL Goldenseal - 6 [hp_X]/mL Lachesis Muta Venom - 10 [hp_X]/mL and more. The currest status of Female Stimulant drug is Active.

Drug Information:

Drug NDC: 43742-1507
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 Stimulant
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: Lilium Tigrinum, Bovista, Cypripedium Pubescens, Hydrastis Canadensis, Petroselinum Sativum, Aquilegia Vulgaris, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Heart (suis), Kreosotum, Oophorinum (suis), Uterus (suis), Folliculinum, Lachesis Mutus, Magnesia Phosphorica, Mercurius Solubilis, Sepia, Pineal Gland (suis), Hypophysis Suis, Aconiticum Acidum Cis-, Apis Venenum Purum, Estradiol, Progesterone, Testosterone, Placenta Totalis Suis, Faecalis (alkaligenes), Mutabile Bacillus (bach)
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:ACONITIC ACID, (Z)- - 10 [hp_X]/mL
ALCALIGENES FAECALIS - 30 [hp_C]/mL
APIS MELLIFERA VENOM - 18 [hp_X]/mL
AQUILEGIA VULGARIS - 8 [hp_X]/mL
CYPRIPEDIUM PARVIFLORUM VAR. PUBESCENS ROOT - 6 [hp_X]/mL
ESCHERICHIA COLI - 30 [hp_C]/mL
ESTRADIOL - 30 [hp_X]/mL
ESTRONE - 8 [hp_X]/mL
GOLDENSEAL - 6 [hp_X]/mL
LACHESIS MUTA VENOM - 10 [hp_X]/mL
LILIUM LANCIFOLIUM WHOLE FLOWERING - 4 [hp_X]/mL
LYCOPERDON UTRIFORME FRUITING BODY - 6 [hp_X]/mL
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE - 10 [hp_X]/mL
MERCURIUS SOLUBILIS - 12 [hp_X]/mL
PETROSELINUM CRISPUM - 6 [hp_X]/mL
PORK HEART - 8 [hp_X]/mL
PROGESTERONE - 30 [hp_X]/mL
SEPIA OFFICINALIS JUICE - 13 [hp_X]/mL
SUS SCROFA ADRENAL GLAND - 8 [hp_X]/mL
SUS SCROFA OVARY - 8 [hp_X]/mL
SUS SCROFA PINEAL GLAND - 16 [hp_X]/mL
SUS SCROFA PITUITARY GLAND - 10 [hp_X]/mL
SUS SCROFA PLACENTA - 6 [hp_C]/mL
SUS SCROFA UMBILICAL CORD - 8 [hp_X]/mL
SUS SCROFA UTERUS - 8 [hp_X]/mL
TESTOSTERONE - 30 [hp_X]/mL
WOOD CREOSOTE - 8 [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: 20 Aug, 2019
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 09 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, 2024
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:M0447348
N0000175825
N0000000100
M0017672
N0000175601
N0000175824
N0000000146
M0001109
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:OF5471ZHRR
05KB30NGW2
76013O881M
8POZ61U1G2
21Y9GZ1LZA
514B9K0L10
4TI98Z838E
2DI9HA706A
ZW3Z11D0JV
VSW71SS07I
X67Z2963PI
K2A74U428F
HF539G9L3Q
324Y4038G2
1WZA4Y92EX
X876KJM95L
4G7DS2Q64Y
QDL83WN8C2
398IYQ16YV
S7YTV04R8O
050QZ2EDK7
L0PFEMQ1DT
C8CV8867O8
118OYG6W3H
2595C75F1P
3XMK78S47O
3JYG22FD73
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 MOA:Estrogen Receptor Agonists [MoA]
Androgen Receptor Agonists [MoA]
Mechanism of action of the drug—molecular, subcellular, or cellular functional activity—of the drug’s established pharmacologic class. Takes the form of the mechanism of action, followed by `[MoA]` (such as `Calcium Channel Antagonists [MoA]` or `Tumor Necrosis Factor Receptor Blocking Activity [MoA]`.
Pharmacologic Class EPC:Estrogen [EPC]
Progesterone [EPC]
Androgen [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 CS:Estradiol Congeners [CS]
Progesterone [CS]
Androstanes [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:Androgen Receptor Agonists [MoA]
Androgen [EPC]
Androstanes [CS]
Calculi Dissolution Agent [EPC]
Estradiol Congeners [CS]
Estrogen Receptor Agonists [MoA]
Estrogen [EPC]
Increased Large Intestinal Motility [PE]
Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]
Magnesium Ion Exchange Activity [MoA]
Osmotic Activity [MoA]
Osmotic Laxative [EPC]
Progesterone [CS]
Progesterone [EPC]
Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.
DEA Schedule:CIII
This is the assigned DEA Schedule number as reported by the labeler. Values are CI, CII, CIII, CIV, and CV.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
43742-1507-130 mL in 1 BOTTLE, DROPPER (43742-1507-1)20 Aug, 2019N/ANo
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.

Purpose:

Homeopathic indications: for temporary relief of symptoms related to female hormonal problems such as fatigue and low energy.** **these statements are based upon traditional homeopathic principles. they have not been reviewed by the food and drug administration.

Product Elements:

Female stimulant lilium tigrinum, bovista, cypripedium pubescens, hydrastis canadensis, petroselinum sativum, aquilegia vulgaris, funiculus umbilicalis suis, glandula suprarenalis suis, heart (suis), kreosotum, oophorinum (suis), uterus (suis), folliculinum, lachesis mutus, magnesia phosphorica, mercurius solubilis, sepia, pineal gland (suis), hypophysis suis, aconiticum acidum cis-, apis venenum purum, estradiol, progesterone, testosterone, placenta totalis suis, faecalis (alkaligenes), mutabile bacillus (bach) lilium lancifolium whole flowering lilium lancifolium whole flowering lycoperdon utriforme fruiting body lycoperdon utriforme fruiting body cypripedium parviflorum var. pubescens root cypripedium parviflorum var. pubescens root goldenseal goldenseal petroselinum crispum petroselinum crispum aquilegia vulgaris aquilegia vulgaris sus scrofa umbilical cord sus scrofa umbilical cord sus scrofa adrenal gland sus scrofa adrenal gland pork heart pork heart wood creosote wood creosote sus scrofa ovary sus scrofa ovary sus scrofa uterus sus scrofa uterus estrone estrone sus scrofa pituitary gland sus scrofa pituitary gland aconitic acid, (z)- aconitic acid, (z)- lachesis muta venom lachesis muta venom magnesium phosphate, dibasic trihydrate magnesium cation mercurius solubilis mercurius solubilis sepia officinalis juice sepia officinalis juice sus scrofa pineal gland sus scrofa pineal gland apis mellifera venom apis mellifera venom estradiol estradiol progesterone progesterone testosterone testosterone sus scrofa placenta sus scrofa placenta alcaligenes faecalis alcaligenes faecalis escherichia coli escherichia coli water alcohol

Indications and Usage:

Homeopathic indications: for temporary relief of symptoms related to female hormonal problems such as fatigue and low energy.** **these statements are based upon traditional homeopathic principles. they have not been reviewed by the food and drug administration.

Warnings:

Warnings: keep out of reach of children. in case of overdose, contact physician or a 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 43742-1507-1 homeopathic female stimulant 1 fl oz (30 ml) female stimulant

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.