NDC 52731-7003 Sinus Complex
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 52731-7003?
What are the uses for Sinus Complex?
Which are Sinus Complex UNII Codes?
The UNII codes for the active ingredients in this product are:
- ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3)
- ANTIMONY (UNII: 9IT35J3UV3) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K)
- EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K) (Active Moiety)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- HEPATICA NOBILIS VAR. OBTUSA (UNII: 6ICN6T7FEM)
- HEPATICA NOBILIS VAR. OBTUSA (UNII: 6ICN6T7FEM) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- MERCURIC SULFIDE (UNII: ZI0T668SF1)
- MERCURIC CATION (UNII: ED30FJ8Y42) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
Which are Sinus Complex 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)
* 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".