NDC 63083-9412 Normal Intestinal Flora Nosode Combination 9412
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What is NDC 63083-9412?
What are the uses for Normal Intestinal Flora Nosode Combination 9412?
Which are Normal Intestinal Flora Nosode Combination 9412 UNII Codes?
The UNII codes for the active ingredients in this product are:
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6)
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (Active Moiety)
- ALOE (UNII: V5VD430YW9)
- ALOE (UNII: V5VD430YW9) (Active Moiety)
- CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17)
- CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- LACTOBACILLUS ACIDOPHILUS (UNII: 1PRR1V42V5)
- LACTOBACILLUS ACIDOPHILUS (UNII: 1PRR1V42V5) (Active Moiety)
- ENTEROBACTER AEROGENES (UNII: 2EIQ8686WC)
- ENTEROBACTER AEROGENES (UNII: 2EIQ8686WC) (Active Moiety)
- ENTEROCOCCUS FAECIUM (UNII: 34YYS7G16P)
- ENTEROCOCCUS FAECIUM (UNII: 34YYS7G16P) (Active Moiety)
- ESCHERICHIA COLI (UNII: 514B9K0L10)
- ESCHERICHIA COLI (UNII: 514B9K0L10) (Active Moiety)
- KLEBSIELLA PNEUMONIAE (UNII: 09PA36CT5R)
- KLEBSIELLA PNEUMONIAE (UNII: 09PA36CT5R) (Active Moiety)
- MERCURIC CHLORIDE (UNII: 53GH7MZT1R)
- MERCURIC CATION (UNII: ED30FJ8Y42) (Active Moiety)
Which are Normal Intestinal Flora Nosode Combination 9412 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".