NDC 43853-0028 Hgh Plus

Alpha Gpc, Deer Antler Velvet, Hepar Suis, Hgh, Igf-1, Igf-2, Pituitarum Post

NDC Product Code 43853-0028

NDC CODE: 43853-0028

Proprietary Name: Hgh Plus 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: Alpha Gpc, Deer Antler Velvet, Hepar Suis, Hgh, Igf-1, Igf-2, Pituitarum Post 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.

  • 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

NDC 43853-0028-1

Package Description: 30 mL in 1 BOTTLE, SPRAY

NDC Product Information

Hgh Plus with NDC 43853-0028 is a a human over the counter drug product labeled by Problen. The generic name of Hgh Plus is alpha gpc, deer antler velvet, hepar suis, hgh, igf-1, igf-2, pituitarum post. The product's dosage form is spray and is administered via oral form.

Labeler Name: Problen

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

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 Plus 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.

  • ALPHA 8 [hp_X]/30mL
  • CERVUS ELAPHUS VELVET 6 [hp_X]/30mL
  • PORK LIVER 6 [hp_X]/30mL
  • SOMATROPIN 12 [hp_X]/30mL
  • DALOTUZUMAB 12 [hp_X]/30mL
  • INSULIN-LIKE GROWTH FACTOR-2 12 [hp_X]/30mL
  • SUS SCROFA PITUITARY GLAND, POSTERIOR 5 [hp_C]/30mL

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.

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

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: Problen
Labeler Code: 43853
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: 05-09-2017 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 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’.

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