NDC 67871-007 Elliotts B
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67871 - Qol Medical, Llc
- 67871-007 - Elliotts B
Product Packages
NDC Code 67871-007-10
Package Description: 10 AMPULE in 1 BOX / 10 mL in 1 AMPULE (67871-007-01)
Product Details
What is NDC 67871-007?
What are the uses for Elliotts B?
Which are Elliotts B UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- BICARBONATE ION (UNII: HN1ZRA3Q20) (Active Moiety)
- ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)
- ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK) (Active Moiety)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- SODIUM PHOSPHATE (UNII: SE337SVY37)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
Which are Elliotts B 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)
* 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".