NDC 63083-9240 Rheum Combination 9240
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63083-9240?
What are the uses for Rheum Combination 9240?
Which are Rheum Combination 9240 UNII Codes?
The UNII codes for the active ingredients in this product are:
- STAR ANISE (UNII: XKC1657P78)
- STAR ANISE (UNII: XKC1657P78) (Active Moiety)
- VERONICASTRUM VIRGINICUM WHOLE (UNII: 1RA4P35F0I)
- VERONICASTRUM VIRGINICUM WHOLE (UNII: 1RA4P35F0I) (Active Moiety)
- MEDICAGO SATIVA WHOLE (UNII: DJO934BRBD)
- MEDICAGO SATIVA WHOLE (UNII: DJO934BRBD) (Active Moiety)
- RHEUM OFFICINALE STEM (UNII: 82X32CRA5U)
- RHEUM OFFICINALE STEM (UNII: 82X32CRA5U) (Active Moiety)
- SENNA LEAF (UNII: AK7JF626KX)
- SENNA LEAF (UNII: AK7JF626KX) (Active Moiety)
- FRANGULA ALNUS BARK (UNII: S2D77IH61R)
- FRANGULA ALNUS BARK (UNII: S2D77IH61R) (Active Moiety)
- ALOE (UNII: V5VD430YW9)
- ALOE (UNII: V5VD430YW9) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17)
- CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (Active Moiety)
- GRAPHITE (UNII: 4QQN74LH4O)
- GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
Which are Rheum Combination 9240 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".