NDC 63083-2060 Sinusitis Drops 2060
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-2060 - Sinusitis Drops
Product Packages
NDC Code 63083-2060-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-2060?
What are the uses for Sinusitis Drops 2060?
Which are Sinusitis Drops 2060 UNII Codes?
The UNII codes for the active ingredients in this product are:
- BLACK MUSTARD SEED (UNII: 8LTY55LQ8D)
- BLACK MUSTARD SEED (UNII: 8LTY55LQ8D) (Active Moiety)
- PULSATILLA MONTANA WHOLE (UNII: 24K790T39B)
- PULSATILLA MONTANA WHOLE (UNII: 24K790T39B) (Active Moiety)
- EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K)
- EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K) (Active Moiety)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
- POTASSIUM DICHROMATE (UNII: T4423S18FM)
- DICHROMATE ION (UNII: 9LKY4BFN2V) (Active Moiety)
- LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU)
- LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- GUAIAC (UNII: 03C8A0DFJ8)
- GUAIAC (UNII: 03C8A0DFJ8) (Active Moiety)
- MERCURIC SULFIDE (UNII: ZI0T668SF1)
- MERCURIC CATION (UNII: ED30FJ8Y42) (Active Moiety)
Which are Sinusitis Drops 2060 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".