NDC 51812-0001 Rejuvenation Hgh
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51812 - Degen Health Products
- 51812-0001 - Rejuvenation
Product Packages
NDC Code 51812-0001-1
Package Description: 60 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 51812-0001?
What are the uses for Rejuvenation Hgh?
Which are Rejuvenation Hgh UNII Codes?
The UNII codes for the active ingredients in this product are:
- FUCUS VESICULOSUS (UNII: 535G2ABX9M)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M) (Active Moiety)
- CYANOCOBALAMIN (UNII: P6YC3EG204)
- CYANOCOBALAMIN (UNII: P6YC3EG204) (Active Moiety)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- PORK LIVER (UNII: 6EC706HI7F)
- PORK LIVER (UNII: 6EC706HI7F) (Active Moiety)
- SUS SCROFA THYROID (UNII: 6RV024OAUQ)
- SUS SCROFA THYROID (UNII: 6RV024OAUQ) (Active Moiety)
- PANCRELIPASE (UNII: FQ3DRG0N5K)
- PANCRELIPASE PROTEASE (UNII: 3560D81V50) (Active Moiety)
- SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79)
- SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79) (Active Moiety)
- SOMATROPIN (UNII: NQX9KB6PCL)
- SOMATROPIN (UNII: NQX9KB6PCL) (Active Moiety)
- SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T)
- SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T) (Active Moiety)
Which are Rejuvenation Hgh Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- WITHANIA SOMNIFERA ROOT (UNII: V038D626IF)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- PFAFFIA PANICULATA ROOT (UNII: KYV09BQ2YN)
- PAULLINIA CUPANA SEED (UNII: C21GE7524R)
- SMILAX REGELII ROOT (UNII: 2H1576D5WG)
- PTYCHOPETALUM OLACOIDES WOOD (UNII: O5XEK0CKFZ)
- ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
- GARCINIA CAMBOGIA FRUIT (UNII: D0QJI8UQVR)
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] 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.
[12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".