NDC 43742-0974 Female Stimulant

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

NDC Product Code 43742-0974

NDC CODE: 43742-0974

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

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • This medication is a female hormone (estrogen). It is used by women to help reduce symptoms of menopause (such as hot flashes, vaginal dryness). These symptoms are caused by the body making less estrogen. If you are using this medication to treat symptoms only in and around the vagina, products applied directly inside the vagina should be considered before medications that are taken by mouth, absorbed through the skin, or injected. This medication may also be used by women who are not able to produce enough estrogen (for example, due to hypogonadism, primary ovarian failure). Certain estrogen products may also be used by women after menopause to prevent bone loss (osteoporosis). However, there are other medications (such as raloxifene, bisphosphonates including alendronate) that are also effective in preventing bone loss and may be safer. These medications should be considered for use before estrogen treatment.
  • Progesterone is a type of female hormone (progestin). This medication is similar to the progesterone that your body naturally makes. It is given to replace the hormone when your body is not making enough of it. In women who are not pregnant and have not gone through menopause, this medication is used to restore normal menstrual periods that have stopped for several months (amenorrhea). It is also used to treat abnormal bleeding from the uterus that is due to low hormone levels and not other causes (e.g., fibroids, cancer of the uterus). Progesterone must not be used to test for pregnancy. Progestins are not effective in preventing miscarriages.
  • This medicated patch contains testosterone. It is used for hormone replacement in men who are not able to produce enough testosterone (e.g., hypogonadism). This medication is absorbed through the skin, enters your bloodstream, and helps your body reach normal testosterone levels. Testosterone helps the body to develop and maintain the male sexual characteristics (masculinity), such as a deep voice and body hair. It also helps to maintain muscle and prevent bone loss, and is necessary for natural sexual ability/desire. This drug should not be used by women.

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-0974-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Female Stimulant with NDC 43742-0974 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Female Stimulant is aquilegia vulgaris, lilium tigrinum, bovista, cypripedium pubescens, hydrastis canadensis, apiolum, apis venenum purum, funiculus umbilicalis suis, glandula suprarenalis suis, heart (suis), kreosotum, oophorinum (suis), uterus (suis), folliculinum, aconiticum acidum, cis-, lachesis mutus, magnesia phosphorica, mercurius solubilis, sepia, pineal gland (suis), hypophysis suis, estradiol, progesterone, testosterone, placenta totalis suis, bacillus faecalis, 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.

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.

  • AQUILEGIA VULGARIS 4 [hp_X]/mL
  • 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
  • APIOLE (PARSLEY) 6 [hp_X]/mL
  • APIS MELLIFERA VENOM 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
  • ACONITIC ACID, (Z)- 10 [hp_X]/mL
  • LACHESIS MUTA VENOM 10 [hp_X]/mL
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 10 [hp_X]/mL
  • MERCURIUS SOLUBILIS 10 [hp_X]/mL
  • SEPIA OFFICINALIS JUICE 10 [hp_X]/mL
  • SUS SCROFA PINEAL GLAND 12 [hp_X]/mL
  • SUS SCROFA PITUITARY GLAND 13 [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.
  • 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: 08-04-2017 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 08-31-2023 What is the End Marketing Date?
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.

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:

Aquilegia Vulgaris 4X, Lilium Tigrinum 4X, Bovista 6X, Cypripedium Pubescens 6X, Hydrastis Canadensis 6X, Apiolum 6X, 10X, 30X, 200X, Apis Venenum Purum 8X, Funiculus Umbilicalis Suis 8X, Glandula Suprarenalis Suis 8X, Heart (Suis) 8X, Kreosotum 8X, Oophorinum (Suis) 8X, Uterus (Suis) 8X, Folliculinum 8X, 30X, 200X, Aconiticum Acidum CIS 10X, Lachesis Mutus 10X, Magnesia Phosphorica 10X, Mercurius Solubilis 10X, Sepia 10X, Pineal Gland (Suis) 12X, Hypophysis Suis 13X, 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 aas 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 aas 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 43742-0974-1HOMEOPATHICFEMALE STIMULANT1 FL OZ (30 ml)

* Please review the disclaimer below.