NDC 57850-2000 Fibrocane Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57850 - Premier Bioceuticals Llc
- 57850-2000 - Fibrocane Relief
Product Packages
NDC Code 57850-2000-1
Package Description: 57 g in 1 TUBE
Product Details
What is NDC 57850-2000?
What are the uses for Fibrocane Relief?
Which are Fibrocane Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
- CAPSICUM (UNII: 00UK7646FG)
- CAPSICUM (UNII: 00UK7646FG) (Active Moiety)
- LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P)
- LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (Active Moiety)
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6)
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (Active Moiety)
- RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U)
- RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U) (Active Moiety)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
Which are Fibrocane Relief 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:
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- CELERY SEED (UNII: 1G1EAA320L)
- COMFREY LEAF (UNII: DG4F8T839X)
- HARPAGOPHYTUM PROCUMBENS ROOT (UNII: 1OYM338E89)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- FEVERFEW (UNII: Z64FK7P217)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- OREGANO (UNII: 0E5AT8T16U)
- POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
- PEG-8 DIMETHICONE (UNII: GIA7T764OD)
- POLYETHYLENE GLYCOL 700 (UNII: 762678AC5R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SORBIC ACID (UNII: X045WJ989B)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WATER (UNII: 059QF0KO0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- TURMERIC (UNII: 856YO1Z64F)
- SALIX ALBA BARK (UNII: 205MXS71H7)
* 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".