NDC 49589-115 Natural Vaginal Care
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49589 - Izun Pharmaceuticals Corporation
- 49589-115 - Natural Vaginal Care
Product Packages
NDC Code 49589-115-60
Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON / 40 g in 1 TUBE, WITH APPLICATOR
Product Details
What is NDC 49589-115?
What are the uses for Natural Vaginal Care?
Which are Natural Vaginal Care 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 Natural Vaginal Care 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:
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- HYPROMELLOSE 2208 (15000 MPA.S) (UNII: Z78RG6M2N2)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- PETROLATUM (UNII: 4T6H12BN9U)
- WATER (UNII: 059QF0KO0R)
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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".