NDC 66096-746 Seagate Olive Leaf
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 66096 - Ohm Pharma Inc.
- 66096-746 - Seagate Olive Leaf
Product Packages
NDC Code 66096-746-09
Package Description: 30 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 66096-746?
Which are Seagate Olive Leaf UNII Codes?
The UNII codes for the active ingredients in this product are:
- BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU)
- BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (Active Moiety)
Which are Seagate Olive Leaf 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:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)
- WATER (UNII: 059QF0KO0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- XYLITOL (UNII: VCQ006KQ1E)
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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".