NDC 71559-301 Nature Knows Allergy Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 71559-301?
Which are Nature Knows Allergy Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- ONION (UNII: 492225Q21H)
- ONION (UNII: 492225Q21H) (Active Moiety)
- AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A)
- AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A) (Active Moiety)
- ARALIA RACEMOSA ROOT (UNII: T90W4582DU)
- ARALIA RACEMOSA ROOT (UNII: T90W4582DU) (Active Moiety)
- JACOBAEA MARITIMA (UNII: U4B223LS4X)
- JACOBAEA MARITIMA (UNII: U4B223LS4X) (Active Moiety)
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
- LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU)
- LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU) (Active Moiety)
- NAPHTHALENE (UNII: 2166IN72UN)
- NAPHTHALENE (UNII: 2166IN72UN) (Active Moiety)
- POPULUS BALSAMIFERA LEAF BUD (UNII: 9CQ6C00G3C)
- POPULUS BALSAMIFERA LEAF BUD (UNII: 9CQ6C00G3C) (Active Moiety)
- QUERCUS ROBUR NUT (UNII: Q7MU1F4GLY)
- QUERCUS ROBUR NUT (UNII: Q7MU1F4GLY) (Active Moiety)
- SALIX NIGRA BARK (UNII: QU52J3A5B3)
- SALIX NIGRA BARK (UNII: QU52J3A5B3) (Active Moiety)
- SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U)
- SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
- ULMUS MINOR FLOWERING TWIG (UNII: J3O020I532)
- ULMUS MINOR FLOWERING TWIG (UNII: J3O020I532) (Active Moiety)
- URTICA URENS (UNII: IHN2NQ5OF9)
- URTICA URENS (UNII: IHN2NQ5OF9) (Active Moiety)
- ANTHOXANTHUM ODORATUM (UNII: YMW1K70E4Q)
- ANTHOXANTHUM ODORATUM (UNII: YMW1K70E4Q) (Active Moiety)
- CANDIDA ALBICANS (UNII: 4D7G21HDBC)
- CANDIDA ALBICANS (UNII: 4D7G21HDBC) (Active Moiety)
Which are Nature Knows Allergy Relief 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".