NDC 50114-1165 Valerianaheel
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 50114-1165?
What are the uses for Valerianaheel?
Which are Valerianaheel UNII Codes?
The UNII codes for the active ingredients in this product are:
- VALERIAN (UNII: JWF5YAW3QW)
- VALERIAN (UNII: JWF5YAW3QW) (Active Moiety)
- TRINITROPHENOL (UNII: A49OS0F91S)
- TRINITROPHENOL (UNII: A49OS0F91S) (Active Moiety)
- PRUNUS SPINOSA FLOWER BUD (UNII: 53Y84VPS2W)
- PRUNUS SPINOSA FLOWER BUD (UNII: 53Y84VPS2W) (Active Moiety)
- HOPS (UNII: 01G73H6H83)
- HOPS (UNII: 01G73H6H83) (Active Moiety)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
- MELISSA OFFICINALIS (UNII: YF70189L0N)
- MELISSA OFFICINALIS (UNII: YF70189L0N) (Active Moiety)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (Active Moiety)
- AMMONIUM BROMIDE (UNII: R0JB3224WS)
- AMMONIUM BROMIDE (UNII: R0JB3224WS) (Active Moiety)
- POTASSIUM BROMIDE (UNII: OSD78555ZM)
- BROMIDE ION (UNII: 952902IX06) (Active Moiety)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- SODIUM BROMIDE (UNII: LC1V549NOM)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
Which are Valerianaheel 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)
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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".