NDC 54118-7972 Ultimate Rescue
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54118 - Abco Laboratories, Inc.
- 54118-7972 - Ultimate Rescue
Product Packages
NDC Code 54118-7972-2
Package Description: 60 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 54118-7972?
What are the uses for Ultimate Rescue?
Which are Ultimate Rescue UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHERRY PLUM (UNII: YSI2ODS7R1)
- CHERRY PLUM (UNII: YSI2ODS7R1) (Active Moiety)
- CLEMATIS CHINENSIS ROOT (UNII: 8Z18N528CU)
- CLEMATIS CHINENSIS ROOT (UNII: 8Z18N528CU) (Active Moiety)
- IMPATIENS BALSAMINA LEAF (UNII: LH9E1X602V)
- IMPATIENS BALSAMINA LEAF (UNII: LH9E1X602V) (Active Moiety)
- CISTUS INCANUS WHOLE (UNII: 22Q313IHPP)
- CISTUS INCANUS WHOLE (UNII: 22Q313IHPP) (Active Moiety)
- ORNITHOGALUM UMBELLATUM (UNII: 9NS3M2Y78S)
- ORNITHOGALUM UMBELLATUM (UNII: 9NS3M2Y78S) (Active Moiety)
- ADENOSINE TRIPHOSPHATE (UNII: 8L70Q75FXE)
- ADENOSINE TRIPHOSPHATE (UNII: 8L70Q75FXE) (Active Moiety)
- BOS TAURUS PINEAL GLAND (UNII: Z7RM5NBH36)
- BOS TAURUS PINEAL GLAND (UNII: Z7RM5NBH36) (Active Moiety)
- BOS TAURUS THYMUS (UNII: 8XEJ88V2T8)
- BOS TAURUS THYMUS (UNII: 8XEJ88V2T8) (Active Moiety)
Which are Ultimate Rescue 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- 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".