NDC 69733-558 Antibacterial Moist Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69733 - Jiangsu Terra Medical Technology Co Ltd
- 69733-558 - Antibacterial Moist Wipes
Product Packages
NDC Code 69733-558-02
Package Description: 20 POUCH in 1 PACKAGE / .00297 g in 1 POUCH
Product Details
What is NDC 69733-558?
What are the uses for Antibacterial Moist Wipes?
Which are Antibacterial Moist 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 Antibacterial Moist 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)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- 2-BROMO-2-NITROETHANOL (UNII: FA22WV2B2Z)
- 2-METHYL-2-PROPYLPROPANE-1,3-DIOL (UNII: YLM5KRU0P4)
- ALOE ARBORESCENS LEAF (UNII: 09TD8L5SQV)
- DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
- TRIETHANOLAMINE BENZOATE (UNII: M3EN4GC19W)
- GLYCERIN (UNII: PDC6A3C0OX)
- TOCOPHERYL RETINOATE (UNII: 0WN694NBMM)
What is the NDC to RxNorm Crosswalk for Antibacterial Moist 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
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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".