NDC 57520-0272 Fibro Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57520 - Apotheca Company
- 57520-0272 - Fibro Relief
Product Characteristics
Product Packages
NDC Code 57520-0272-1
Package Description: 120 CAPSULE in 1 BOTTLE
Product Details
What is NDC 57520-0272?
What are the uses for Fibro Relief?
Which are Fibro Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- IRON (UNII: E1UOL152H7)
- IRON (UNII: E1UOL152H7) (Active Moiety)
- GUAIACUM OFFICINALE RESIN (UNII: N0K2Z502R6)
- GUAIACUM OFFICINALE RESIN (UNII: N0K2Z502R6) (Active Moiety)
- LITHIUM CARBONATE (UNII: 2BMD2GNA4V)
- LITHIUM CATION (UNII: 8H8Z5UER66) (Active Moiety)
- TOMATO (UNII: Z4KHF2C175)
- TOMATO (UNII: Z4KHF2C175) (Active Moiety)
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
Which are Fibro 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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- NYMPHAEA ODORATA ROOT (UNII: 69RAZ4C432)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- MARSDENIA CONDURANGO BARK (UNII: R23QIR6YBA)
- ELYMUS REPENS ROOT (UNII: 3IXW0F6P8W)
- EUROPEAN ELDERBERRY (UNII: BQY1UBX046)
- LOBELIA INFLATA (UNII: 9PP1T3TC5U)
- RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C)
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[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".