NDC 68121-003 Home Formation Antibacterial Coconut And Hibiscus
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68121 - Patcos Cosmetics (india) Private Limited
- 68121-003 - Home Formation Antibacterial Coconut And Hibiscus
Product Packages
NDC Code 68121-003-01
Package Description: 333 mL in 1 BOTTLE
Product Details
What is NDC 68121-003?
What are the uses for Home Formation Antibacterial Coconut And Hibiscus?
Which are Home Formation Antibacterial Coconut And Hibiscus UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Home Formation Antibacterial Coconut And Hibiscus 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:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
- BRONOPOL (UNII: 6PU1E16C9W)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BENZOPHENONE (UNII: 701M4TTV9O)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- WATER (UNII: 059QF0KO0R)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- LAURETH-10 (UNII: BD7AST04GA)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
What is the NDC to RxNorm Crosswalk for Home Formation Antibacterial Coconut And Hibiscus?
- 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".