NDC 0220-9341 Sinusalia
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0220 - Laboratoires Boiron
- 0220-9341 - Sinusalia
Product Characteristics
Product Packages
NDC Code 0220-9341-04
Package Description: 60 TABLET in 1 BLISTER PACK
Product Details
What is NDC 0220-9341?
What are the uses for Sinusalia?
Which are Sinusalia UNII Codes?
The UNII codes for the active ingredients in this product are:
- BELLADONNA LEAF (UNII: 6GZW20TIOI)
- BELLADONNA LEAF (UNII: 6GZW20TIOI) (Active Moiety)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (Active Moiety)
- SPIGELIA MARILANDICA ROOT (UNII: 467D26HS0B)
- SPIGELIA MARILANDICA ROOT (UNII: 467D26HS0B) (Active Moiety)
Which are Sinusalia 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:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
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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".