NDC 60512-9056 Fibromyalgia Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 60512 - Homeolab Usa Inc.
- 60512-9056 - Fibromyalgia Relief
Product Characteristics
Product Packages
NDC Code 60512-9056-1
Package Description: 80 PELLET in 1 TUBE
Product Details
What is NDC 60512-9056?
What are the uses for Fibromyalgia Relief?
Which are Fibromyalgia Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM PHOSPHATE (UNII: 97Z1WI3NDX)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (Active Moiety)
- CAUSTICUM (UNII: DD5FO1WKFU)
- CAUSTICUM (UNII: DD5FO1WKFU) (Active Moiety)
- TOXICODENDRON RADICANS LEAF (UNII: CDH3461U7L)
- TOXICODENDRON RADICANS LEAF (UNII: CDH3461U7L) (Active Moiety)
- MAGNESIUM PHOSPHATE, DIBASIC (UNII: A1Y870209Z)
- MAGNESIUM PHOSPHATE, DIBASIC (UNII: A1Y870209Z) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
- LYTTA VESICATORIA (UNII: 3Q034RO3BT)
- LYTTA VESICATORIA (UNII: 3Q034RO3BT) (Active Moiety)
- POTASSIUM DICHROMATE (UNII: T4423S18FM)
- DICHROMATE ION (UNII: 9LKY4BFN2V) (Active Moiety)
Which are Fibromyalgia 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:
- SUCROSE (UNII: C151H8M554)
- LACTOSE (UNII: J2B2A4N98G)
* 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".