NDC 63083-4017 Allergy Nosode 4017
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 63083-4017?
What are the uses for Allergy Nosode 4017?
Which are Allergy Nosode 4017 UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOUSE DUST (UNII: EYO007VX98)
- HOUSE DUST (UNII: EYO007VX98) (Active Moiety)
- STACHYBOTRYS CHARTARUM (UNII: HJ4L70T1ZP)
- STACHYBOTRYS CHARTARUM (UNII: HJ4L70T1ZP) (Active Moiety)
- MEDICAGO SATIVA WHOLE (UNII: DJO934BRBD)
- MEDICAGO SATIVA WHOLE (UNII: DJO934BRBD) (Active Moiety)
- FRAXINUS LATIFOLIA WHOLE (UNII: 024W88F557)
- FRAXINUS LATIFOLIA WHOLE (UNII: 024W88F557) (Active Moiety)
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
- POTASSIUM DICHROMATE (UNII: T4423S18FM)
- DICHROMATE ION (UNII: 9LKY4BFN2V) (Active Moiety)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
- HISTAMINE (UNII: 820484N8I3)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- GUAIAC (UNII: 03C8A0DFJ8)
- GUAIAC (UNII: 03C8A0DFJ8) (Active Moiety)
- LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU)
- LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU) (Active Moiety)
Which are Allergy Nosode 4017 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".