NDC 69779-028 Energy And Motivation
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 69779-028?
What are the uses for Energy And Motivation?
Which are Energy And Motivation UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM SULFATE ANHYDROUS (UNII: E934B3V59H)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- GENTIANELLA AMARELLA FLOWER (UNII: ZKH2SOY1AR)
- GENTIANELLA AMARELLA FLOWER (UNII: ZKH2SOY1AR) (Active Moiety)
- DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
- OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ)
- OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- ULEX EUROPAEUS FLOWER (UNII: 398DBS1PXN)
- ULEX EUROPAEUS FLOWER (UNII: 398DBS1PXN) (Active Moiety)
Which are Energy And Motivation 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:
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- CEDAR LEAF OIL (UNII: BJ169U4NLG)
- COMFREY (UNII: D05HXK6R3G)
- LUFFA (UNII: F0R3Y60C6V)
- PENNYROYAL OIL (UNII: AK85U7Y3MV)
- ACHILLEA MILLEFOLIUM FLOWERING TOP (UNII: 55862Q3XEU)
- WATER (UNII: 059QF0KO0R)
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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".