NDC 63083-2152 Sleep Disorder Drops 2152
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 63083-2152?
What are the uses for Sleep Disorder Drops 2152?
Which are Sleep Disorder Drops 2152 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARTEMISIA ANNUA FLOWERING TOP (UNII: 0UQK6O82OW)
- ARTEMISIA ANNUA FLOWERING TOP (UNII: 0UQK6O82OW) (Active Moiety)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- ASIAN GINSENG (UNII: CUQ3A77YXI) (Active Moiety)
- PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O)
- PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O) (Active Moiety)
- SCHISANDRIN B, (+/-)- (UNII: 02XA4X3KZW)
- SCHISANDRIN B, (+/-)- (UNII: 02XA4X3KZW) (Active Moiety)
- AMBER (UNII: 70J9Z0J26P)
- AMBER (UNII: 70J9Z0J26P) (Active Moiety)
- RAUWOLFIA SERPENTINA (UNII: H192N84N1G)
- RAUWOLFIA SERPENTINA (UNII: H192N84N1G) (Active Moiety)
- GRAPHITE (UNII: 4QQN74LH4O)
- GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
- ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD)
- ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD) (Active Moiety)
- BARIUM CARBONATE (UNII: 6P669D8HQ8)
- BARIUM CATION (UNII: V645272HLN) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (Active Moiety)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)
Which are Sleep Disorder Drops 2152 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:
- ALCOHOL (UNII: 3K9958V90M)
- 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".