NDC 63776-074 Candida Plus
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 63776-074?
What are the uses for Candida Plus?
Which are Candida Plus UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMMONIAC (UNII: 8471AK50P8)
- AMMONIAC (UNII: 8471AK50P8) (Active Moiety)
- ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6)
- ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (Active Moiety)
- CAFFEIC ACID (UNII: U2S3A33KVM)
- CAFFEIC ACID (UNII: U2S3A33KVM) (Active Moiety)
- CANDIDA ALBICANS (UNII: 4D7G21HDBC)
- CANDIDA ALBICANS (UNII: 4D7G21HDBC) (Active Moiety)
- CANDIDA PARAPSILOSIS (UNII: 0KZ676D44N)
- CANDIDA PARAPSILOSIS (UNII: 0KZ676D44N) (Active Moiety)
- IPECAC (UNII: 62I3C8233L)
- IPECAC (UNII: 62I3C8233L) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- YEAST MANNAN (UNII: 91R887N59P)
- YEAST MANNAN (UNII: 91R887N59P) (Active Moiety)
- VACCINIUM VITIS-IDAEA LEAF (UNII: FO2ACM0RMQ)
- VACCINIUM VITIS-IDAEA LEAF (UNII: FO2ACM0RMQ) (Active Moiety)
Which are Candida Plus 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)
* Please review the disclaimer below.
[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".