NDC 63083-9258 Rauwolfia Combination 9258
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What is NDC 63083-9258?
What are the uses for Rauwolfia Combination 9258?
Which are Rauwolfia Combination 9258 UNII Codes?
The UNII codes for the active ingredients in this product are:
- HAWTHORN LEAF WITH FLOWER (UNII: 6OM09RPY36)
- HAWTHORN LEAF WITH FLOWER (UNII: 6OM09RPY36) (Active Moiety)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
- AVISCUMINE (UNII: 4B18YVW82N)
- AVISCUMINE (UNII: 4B18YVW82N) (Active Moiety)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW) (Active Moiety)
- KALMIA LATIFOLIA LEAF (UNII: 79N6542N18)
- KALMIA LATIFOLIA LEAF (UNII: 79N6542N18) (Active Moiety)
- AMARYLLIS BELLADONNA WHOLE (UNII: 11B89M58UN)
- AMARYLLIS BELLADONNA WHOLE (UNII: 11B89M58UN) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- RAUWOLFIA SERPENTINA (UNII: H192N84N1G)
- RAUWOLFIA SERPENTINA (UNII: H192N84N1G) (Active Moiety)
- ARTICHOKE (UNII: 4F3W47PLBE)
- ARTICHOKE (UNII: 4F3W47PLBE) (Active Moiety)
- MELILOTUS OFFICINALIS TOP (UNII: GM6P02J2DX)
- MELILOTUS OFFICINALIS TOP (UNII: GM6P02J2DX) (Active Moiety)
- GOLD MONOIODIDE (UNII: T1UDV7ES1A)
- GOLD MONOIODIDE (UNII: T1UDV7ES1A) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Rauwolfia Combination 9258 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".