NDC 63083-9233 Mercurius Combination 9233
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 63083-9233?
What are the uses for Mercurius Combination 9233?
Which are Mercurius Combination 9233 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AILANTHUS ALTISSIMA FLOWERING TWIG (UNII: 8P29O5P7XU)
- AILANTHUS ALTISSIMA FLOWERING TWIG (UNII: 8P29O5P7XU) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8) (Active Moiety)
- AMARYLLIS BELLADONNA WHOLE (UNII: 11B89M58UN)
- AMARYLLIS BELLADONNA WHOLE (UNII: 11B89M58UN) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- HUMAN HERPESVIRUS 1 (UNII: 22G38P19RL)
- HUMAN HERPESVIRUS 1 (UNII: 22G38P19RL) (Active Moiety)
- RECOMBINANT VARICELLA ZOSTER VIRUS GLYCOPROTEIN E ANTIGEN (UNII: COB9FF6I46)
- RECOMBINANT VARICELLA ZOSTER VIRUS GLYCOPROTEIN E ANTIGEN (UNII: COB9FF6I46) (Active Moiety)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (Active Moiety)
Which are Mercurius Combination 9233 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".