NDC 51885-3150 Sinusin
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Product Details
What is NDC 51885-3150?
What are the uses for Sinusin?
Which are Sinusin UNII Codes?
The UNII codes for the active ingredients in this product are:
- PULSATILLA VULGARIS (UNII: I76KB35JEV)
- PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
- EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K)
- EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K) (Active Moiety)
- LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU)
- LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU) (Active Moiety)
- MERCURIC IODIDE (UNII: R03O05RB0P)
- MERCURIC IODIDE (UNII: R03O05RB0P) (Active Moiety)
- SUS SCROFA NASAL MUCOSA (UNII: ID3Z1X61WY)
- SUS SCROFA NASAL MUCOSA (UNII: ID3Z1X61WY) (Active Moiety)
- SILVER NITRATE (UNII: 95IT3W8JZE)
- SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q)
- SULFATE ION (UNII: 7IS9N8KPMG) (Active Moiety)
- SINUSITISINUM (UNII: B575563DM5)
- SINUSITISINUM (UNII: B575563DM5) (Active Moiety)
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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".