NDC 49589-199 Periactive
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49589 - Izun Pharmaceuticals Corp
- 49589-199 - Periactive
Product Packages
NDC Code 49589-199-10
Package Description: 100 mL in 1 BOTTLE
NDC Code 49589-199-50
Package Description: 12 BOTTLE in 1 CARTON / 500 mL in 1 BOTTLE
Product Details
What is NDC 49589-199?
What are the uses for Periactive?
Which are Periactive UNII Codes?
The UNII codes for the active ingredients in this product are:
- SAMBUCUS NIGRA FLOWER (UNII: 07V4DX094T)
- SAMBUCUS NIGRA FLOWER (UNII: 07V4DX094T) (Active Moiety)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- ECHINACEA PURPUREA (UNII: QI7G114Y98) (Active Moiety)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- CENTELLA ASIATICA (UNII: 7M867G6T1U) (Active Moiety)
Which are Periactive 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:
- CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SORBITOL (UNII: 506T60A25R)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- WATER (UNII: 059QF0KO0R)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
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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".