NDC 43772-0030 Nerve Plus Composition
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43772 - Synergy Formulas, Inc.
- 43772-0030 - Nerve Plus Composition
Product Packages
NDC Code 43772-0030-1
Package Description: 60 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43772-0030?
What are the uses for Nerve Plus Composition?
Which are Nerve Plus Composition UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMANITA MUSCARIA FRUITING BODY (UNII: DIF093I037)
- AMANITA MUSCARIA FRUITING BODY (UNII: DIF093I037) (Active Moiety)
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV) (Active Moiety)
- PORK BRAIN (UNII: 466251J72G)
- PORK BRAIN (UNII: 466251J72G) (Active Moiety)
- LEAD (UNII: 2P299V784P)
- LEAD (UNII: 2P299V784P) (Active Moiety)
- NAJA NAJA VENOM (UNII: ZZ4AG7L7VM)
- NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
Which are Nerve Plus Composition 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:
- 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".