NDC 57520-0556 Compre Tox
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57520 - Apotheca Company
- 57520-0556 - Compre Tox
Product Packages
NDC Code 57520-0556-1
Package Description: 60 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 57520-0556?
What are the uses for Compre Tox?
Which are Compre Tox UNII Codes?
The UNII codes for the active ingredients in this product are:
- ERIODICTYON CALIFORNICUM LEAF (UNII: 2Y7TIQ135H)
- ERIODICTYON CALIFORNICUM LEAF (UNII: 2Y7TIQ135H) (Active Moiety)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
- NYMPHAEA ODORATA ROOT (UNII: 69RAZ4C432)
- NYMPHAEA ODORATA ROOT (UNII: 69RAZ4C432) (Active Moiety)
- PLANTAGO MAJOR (UNII: W2469WNO6U)
- PLANTAGO MAJOR (UNII: W2469WNO6U) (Active Moiety)
- ZANTHOXYLUM AMERICANUM BARK (UNII: A4KL1HMZ7T)
- ZANTHOXYLUM AMERICANUM BARK (UNII: A4KL1HMZ7T) (Active Moiety)
- XEROPHYLLUM ASPHODELOIDES (UNII: 9I4XB1GP2B)
- XEROPHYLLUM ASPHODELOIDES (UNII: 9I4XB1GP2B) (Active Moiety)
- YUCCA FILAMENTOSA (UNII: T6VR38UJ9I)
- YUCCA FILAMENTOSA (UNII: T6VR38UJ9I) (Active Moiety)
- GINGER (UNII: C5529G5JPQ)
- GINGER (UNII: C5529G5JPQ) (Active Moiety)
Which are Compre Tox 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".