NDC 63083-2103 Large Intestine Formula 2103
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 63083-2103?
What are the uses for Large Intestine Formula 2103?
Which are Large Intestine Formula 2103 UNII Codes?
The UNII codes for the active ingredients in this product are:
- SCLEROMITRION DIFFUSUM WHOLE (UNII: 291PPU5K9I)
- SCLEROMITRION DIFFUSUM WHOLE (UNII: 291PPU5K9I) (Active Moiety)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357) (Active Moiety)
- SANGUISORBA OFFICINALIS ROOT (UNII: 4NYV2HT01X)
- SANGUISORBA OFFICINALIS ROOT (UNII: 4NYV2HT01X) (Active Moiety)
- MAGNOLIA OFFICINALIS BARK (UNII: 5M609NV974)
- MAGNOLIA OFFICINALIS BARK (UNII: 5M609NV974) (Active Moiety)
- STYPHNOLOBIUM JAPONICUM FLOWER (UNII: 644C3CSB6E)
- STYPHNOLOBIUM JAPONICUM FLOWER (UNII: 644C3CSB6E) (Active Moiety)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) (Active Moiety)
- LONICERA HYPOGLAUCA FLOWER (UNII: 3ADI26ATFY)
- LONICERA HYPOGLAUCA FLOWER (UNII: 3ADI26ATFY) (Active Moiety)
- TARAXACUM SINICUM WHOLE (UNII: 11982A05XX)
- TARAXACUM SINICUM WHOLE (UNII: 11982A05XX) (Active Moiety)
- ANGELICA GIGAS ROOT (UNII: 32766B2FHX)
- ANGELICA GIGAS ROOT (UNII: 32766B2FHX) (Active Moiety)
Which are Large Intestine Formula 2103 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".