NDC 72133-431 Personal Care Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72133 - Delta Brands & Products, Llc
- 72133-431 - Personal Care
Product Packages
NDC Code 72133-431-30
Package Description: 30 CLOTH in 1 PACKAGE
NDC Code 72133-431-40
Package Description: 40 CLOTH in 1 PACKAGE
Product Details
What is NDC 72133-431?
What are the uses for Personal Care Wipes?
Which are Personal Care Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Personal Care Wipes 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- EDETATE SODIUM (UNII: MP1J8420LU)
- CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
What is the NDC to RxNorm Crosswalk for Personal Care Wipes?
- RxCUI: 1038856 - benzalkonium Cl 0.1 % Medicated Pad
- RxCUI: 1038856 - benzalkonium chloride 1 MG/ML Medicated Pad
- RxCUI: 1038856 - benzalkonium chloride 0.1 % Medicated Wipes
- RxCUI: 1038856 - benzalkonium chloride 0.1 % Topical Swab
* Please review the disclaimer below.
[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".