NDC 50563-232 Livegreen Lemon Verbena Antibacterial Foaming Hand Wash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50563 - Enchante Accessories Inc.
- 50563-232 - Livegreen Lemon Verbena Antibacterial Foaming Hand Wash
Product Packages
NDC Code 50563-232-01
Package Description: 500 mL in 1 BOTTLE
Product Details
What is NDC 50563-232?
What are the uses for Livegreen Lemon Verbena Antibacterial Foaming Hand Wash?
Which are Livegreen Lemon Verbena Antibacterial Foaming Hand Wash UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Livegreen Lemon Verbena Antibacterial Foaming Hand Wash 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:
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- DISODIUM HEDTA (UNII: KME849MC7A)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- VERBENA OFFICINALIS (UNII: QT8A71T9BM)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Livegreen Lemon Verbena Antibacterial Foaming Hand Wash?
- RxCUI: 1046593 - benzalkonium chloride 0.13 % Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap
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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".