NDC 51209-016 Dalan Therapy Antibacterial Hand Wash, Fresh Protection
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51209 - Dalan Kimya Endustri Anonim Sirketi
- 51209-016 - Dalan Therapy Antibacterial Hand Wash, Fresh Protection
Product Packages
NDC Code 51209-016-00
Package Description: 300 mL in 1 BOTTLE
Product Details
What is NDC 51209-016?
What are the uses for Dalan Therapy Antibacterial Hand Wash, Fresh Protection?
Which are Dalan Therapy Antibacterial Hand Wash, Fresh Protection UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Dalan Therapy Antibacterial Hand Wash, Fresh Protection 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:
- WATER (UNII: 059QF0KO0R)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
- COCAMINE OXIDE (UNII: QWA2IZI6FI)
- COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GLYCERIN (UNII: PDC6A3C0OX)
- LACTIC ACID (UNII: 33X04XA5AT)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
- EDETATE SODIUM (UNII: MP1J8420LU)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- TRIETHYLENE GLYCOL (UNII: 3P5SU53360)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Dalan Therapy Antibacterial Hand Wash, Fresh Protection?
- 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".