NDC 43742-0988 Hgh Vitality

Agnus Castus, Ambra Grisea, Conium Maculatum, Apiolum, Estradiol, Estriol, Folliculinum, L-dopa, Melatonin, Testosterone, Adenosinum Triphosphoricum Dinatrum, Alpha-lipoicum Acidum, Nadidum, Pantothenic Acid, Sarcolacticum Acidum, Ubidecarenonum, Baryta Carbonica, Selenium Metallicum, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Hepar Suis, Hypothalamus (suis), Lymph Node (suis), Medulla Ossis Suis, Oophorinum (suis), Orchitinum (suis), Pancreas Suis, Spleen (suis), Human Growth Hormone

NDC Product Code 43742-0988

NDC CODE: 43742-0988

Proprietary Name: Hgh Vitality 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: Agnus Castus, Ambra Grisea, Conium Maculatum, Apiolum, Estradiol, Estriol, Folliculinum, L-dopa, Melatonin, Testosterone, Adenosinum Triphosphoricum Dinatrum, Alpha-lipoicum Acidum, Nadidum, Pantothenic Acid, Sarcolacticum Acidum, Ubidecarenonum, Baryta Carbonica, Selenium Metallicum, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Hepar Suis, Hypothalamus (suis), Lymph Node (suis), Medulla Ossis Suis, Oophorinum (suis), Orchitinum (suis), Pancreas Suis, Spleen (suis), Human Growth Hormone 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.
  • Melatonin has been used for short-term treatment of trouble sleeping (insomnia) due to sleep cycle disorders and time changes (jet lag). This product may help you fall asleep faster and decrease the number of times you awaken during the night. It may also help you sleep for a longer time. Melatonin is a substance that your body normally makes. It is thought to help your body's regular daily cycle, hormone production, and sleep patterns. Some herbal/diet supplement products have been found to contain possibly harmful impurities/additives. Check with your pharmacist for more details regarding the particular brand you use. The FDA has not reviewed this product for safety or effectiveness. Consult your doctor or pharmacist for more details.
  • 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.
  • Coenzyme Q10 has been used for heart problems (e.g., heart failure, angina), high blood pressure, Parkinson's disease, gum disease, and certain diseases passed down through families (Huntington's disease, muscular dystrophy). It has also been used for reducing the number of migraine headaches and for reducing cell damage that may occur after surgery or treatment with certain anti-cancer drugs. If you have or think you have any of the conditions listed above, consult your doctor for advice on proper care and treatment. Coenzyme Q10 is a substance that your body normally makes. Your body uses it to help keep in good health. Some herbal/diet supplement products have been found to contain possibly harmful impurities/additives. Check with your pharmacist for more details about the brand you use. The FDA has not reviewed this product for safety or effectiveness. Consult your doctor or pharmacist for more details.
  • Drug uses not available
  • Various brands of this medication are used for the treatment of one of the following medical conditions: growth failure, growth hormone deficiency, intestinal disorder (short bowel syndrome) or HIV-related weight loss or wasting. Somatropin is also used to increase height in children with certain disorders (such as Noonan syndrome, Turner syndrome, idiopathic short stature).

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-0988-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Hgh Vitality with NDC 43742-0988 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Hgh Vitality is agnus castus, ambra grisea, conium maculatum, apiolum, estradiol, estriol, folliculinum, l-dopa, melatonin, testosterone, adenosinum triphosphoricum dinatrum, alpha-lipoicum acidum, nadidum, pantothenic acid, sarcolacticum acidum, ubidecarenonum, baryta carbonica, selenium metallicum, funiculus umbilicalis suis, glandula suprarenalis suis, hepar suis, hypothalamus (suis), lymph node (suis), medulla ossis suis, oophorinum (suis), orchitinum (suis), pancreas suis, spleen (suis), human growth hormone. 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.

Hgh Vitality 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.

  • CHASTE TREE 6 [hp_X]/mL
  • AMBERGRIS 6 [hp_X]/mL
  • CONIUM MACULATUM FLOWERING TOP 6 [hp_X]/mL
  • APIOLE (PARSLEY) 6 [hp_X]/mL
  • ESTRADIOL 6 [hp_X]/mL
  • ESTRIOL 6 [hp_X]/mL
  • ESTRONE 6 [hp_X]/mL
  • LEVODOPA 6 [hp_X]/mL
  • MELATONIN 6 [hp_X]/mL
  • TESTOSTERONE 6 [hp_X]/mL
  • ADENOSINE TRIPHOSPHATE DISODIUM 8 [hp_X]/mL
  • .ALPHA.-LIPOIC ACID 8 [hp_X]/mL
  • NADIDE 8 [hp_X]/mL
  • PANTOTHENIC ACID 8 [hp_X]/mL
  • LACTIC ACID, L- 8 [hp_X]/mL
  • UBIDECARENONE 8 [hp_X]/mL
  • BARIUM CARBONATE 8 [hp_X]/mL
  • SELENIUM 8 [hp_X]/mL
  • SUS SCROFA UMBILICAL CORD 30 [hp_X]/mL
  • SUS SCROFA ADRENAL GLAND 30 [hp_X]/mL
  • PORK LIVER 30 [hp_X]/mL
  • SUS SCROFA HYPOTHALAMUS 30 [hp_X]/mL
  • SUS SCROFA LYMPH 30 [hp_X]/mL
  • SUS SCROFA BONE MARROW 30 [hp_X]/mL
  • SUS SCROFA OVARY 30 [hp_X]/mL
  • SUS SCROFA TESTICLE 30 [hp_X]/mL
  • SUS SCROFA PANCREAS 30 [hp_X]/mL
  • SUS SCROFA SPLEEN 30 [hp_X]/mL
  • SOMATROPIN 30 [hp_X]/mL
  • PROTEUS MORGANII 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: 03-03-2017 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: 07-13-2023 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.

Hgh Vitality Product Label Images

Hgh Vitality 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:

Agnus Castus 6X, 12X, 30X, Ambra Grisea 6X, 12X, 30X, Conium Maculatum 6X, 12X, 30X, Apiolum 6X, 12X, 30X, 200X, 12C, 30C , 60C, 200C, Estradiol 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Estriol 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Folliculinum 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, L-Dopa 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Melatonin 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Testosterone 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Adenosinum Triphosphoricum Dinatrum 8X, Alpha-Lipoicum Acidum 8X, Nadidum 8X, Pantothenic Acid 8X, Sarcolacticum Acidum 8X, Ubidecarenonum 8X, Baryta Carbonica 8X, 12X, 30X, Selenium Metallicum 8X, 12X, 30X, Funiculus Umbilicalis Suis 30X, Glandula Suprarenalis Suis 30X, Hepar Suis 30X, Hypothalamus (Suis) 30X, Lymph Node (Suis) 30X, Medulla Ossis Suis 30X, Oophorinum (Suis) 30X, Orchitinum (Suis) 30X, Pancreas Suis 30X, Spleen (Suis) 30X, Human Growth Hormone 30X, 60X, 200X, Proteus (Morgani) 30C.

Homeopathic Indications:

For temporary relief of symptoms related to aging including fatigue, minor joint pain and muscle soreness.****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 aging including fatigue, minor joint pain and muscle soreness.****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, get medical help or contact 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, get medical help or contact a Poison Control Center right away.

Directions:

10 drops under the tongue, three times per 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 Drive • Sandy, UT 84070www.desbio.com

Package Label Display:

DESBIONDC 43742-0988-1HOMEOPATHICHGHVitality1 FL OZ (30 ml)

* Please review the disclaimer below.