NDC 43742-1507 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)

NDC Product Code 43742-1507

NDC Code: 43742-1507

Proprietary Name: Female Stimulant What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

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) What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-1507-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Female Stimulant with NDC 43742-1507 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Female Stimulant is 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). The product's dosage form is liquid and is administered via oral form.

Labeler Name: Deseret Biologicals, Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

DEA Schedule: Schedule III (CIII) Substances What is the Drug Enforcement Administration (DEA) CIII Schedule?
The controlled substances in the CIII schedule have an abuse potential and dependence liability less than those in schedules CI and CII, and have an accepted medical use in the United States. Schedule CIII controlled substances include preparations containing limited quantities of certain narcotic drugs, and other nonnarcotic drugs such as: derivatives of barbituric acid, except those that are listed in another schedule, glutethimide (Doriden), methyprylon (Noludar), nalorphine, benzphetamine, chlorphentermine, clortermine, and phendimetrazine.

Female Stimulant Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • LILIUM LANCIFOLIUM WHOLE FLOWERING 4 [hp_X]/mL
  • LYCOPERDON UTRIFORME FRUITING BODY 6 [hp_X]/mL
  • CYPRIPEDIUM PARVIFLORUM VAR. PUBESCENS ROOT 6 [hp_X]/mL
  • GOLDENSEAL 6 [hp_X]/mL
  • PETROSELINUM CRISPUM 6 [hp_X]/mL
  • AQUILEGIA VULGARIS 8 [hp_X]/mL
  • SUS SCROFA UMBILICAL CORD 8 [hp_X]/mL
  • SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL
  • PORK HEART 8 [hp_X]/mL
  • WOOD CREOSOTE 8 [hp_X]/mL
  • SUS SCROFA OVARY 8 [hp_X]/mL
  • SUS SCROFA UTERUS 8 [hp_X]/mL
  • ESTRONE 8 [hp_X]/mL
  • SUS SCROFA PITUITARY GLAND 10 [hp_X]/mL
  • ACONITIC ACID, (Z)- 10 [hp_X]/mL
  • LACHESIS MUTA VENOM 10 [hp_X]/mL
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 10 [hp_X]/mL
  • MERCURIUS SOLUBILIS 12 [hp_X]/mL
  • SEPIA OFFICINALIS JUICE 13 [hp_X]/mL
  • SUS SCROFA PINEAL GLAND 16 [hp_X]/mL
  • APIS MELLIFERA VENOM 18 [hp_X]/mL
  • ESTRADIOL 30 [hp_X]/mL
  • PROGESTERONE 30 [hp_X]/mL
  • TESTOSTERONE 30 [hp_X]/mL
  • SUS SCROFA PLACENTA 6 [hp_C]/mL
  • ALCALIGENES FAECALIS 30 [hp_C]/mL
  • ESCHERICHIA COLI 30 [hp_C]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Deseret Biologicals, Inc.
Labeler Code: 43742
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/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.

Start Marketing Date: 08-20-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Female Stimulant Product Label Images

Female Stimulant Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Lilium Tigrinum 4X, Bovista 6X, Cypripedium Pubescens 6X, Hydrastis Canadensis 6X, Petroselinum Sativum 6X, 10X, 30X, 200X, Aquilegia Vulgaris 8X, Funiculus Umbilicalis Suis 8X, Glandula Suprarenalis Suis 8X, Heart (Suis) 8X, Kreosotum 8X, Oophorinum (Suis) 8X, Uterus (Suis) 8X, Folliculinum 8X, 30X, 200X, Lachesis Mutus 10X, Magnesia Phosphorica 10X, Mercurius Solubilis 10X, Sepia 10X, Pineal Gland (Suis) 12X, Hypophysis Suis 13X, Aconiticum Acidum CIS 16X, Apis Venenum Purum 18X, Estradiol 30X, 60X, 200X, Progesterone 30X, 60X, 200X, Testosterone 30X, 60X, 200X, Placenta Totalis Suis 6C, Bacillus Faecalis 30C, 200C, Mutabile Bacillus (Bach) 30C, 200C.

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.

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:

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.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.

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.

Inactive Ingredients:

Demineralized Water, 25% Ethanol

Questions:

Dist. By: Deseret Biologicals, Inc.469 W. Parkland DriveSandy, UT 84070 www.desbio.com

Package Label Display:

DESBIONDC 43742-1507-1HOMEOPATHICFEMALESTIMULANT1 FL OZ (30 ml)

* Please review the disclaimer below.