NDC 77418-202 Abutol Antiseptic Hand Wash Lavender And Jasmine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77418 - Atak Farma Kozmetik Ve Kimya Sanayi Ticaret Anonim Sirketi
- 77418-202 - Abutol Antiseptic Hand Wash Lavender And Jasmine
Product Packages
NDC Code 77418-202-20
Package Description: 500 mL in 1 BOTTLE
Product Details
What is NDC 77418-202?
What are the uses for Abutol Antiseptic Hand Wash Lavender And Jasmine?
Which are Abutol Antiseptic Hand Wash Lavender And Jasmine UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Abutol Antiseptic Hand Wash Lavender And Jasmine 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)
- SULISOBENZONE (UNII: 1W6L629B4K)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
- EDETATE SODIUM (UNII: MP1J8420LU)
What is the NDC to RxNorm Crosswalk for Abutol Antiseptic Hand Wash Lavender And Jasmine?
- RxCUI: 1053188 - benzalkonium chloride 0.12 % Medicated Liquid Soap
- RxCUI: 1053188 - benzalkonium chloride 1.2 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".