NDC 52489-421 Sanitizing Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52489 - Imperial Palace Commodity (shenzhen) Co., Ltd
- 52489-421 - Sanitizing Wipes
Product Packages
NDC Code 52489-421-01
Package Description: 800 NOT APPLICABLE in 1 BAG / 800 mL in 1 NOT APPLICABLE
NDC Code 52489-421-02
Package Description: 800 NOT APPLICABLE in 1 CANISTER / 800 mL in 1 NOT APPLICABLE
Product Details
What is NDC 52489-421?
What are the uses for Sanitizing Wipes?
Which are Sanitizing 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 Sanitizing 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:
- CHLORPHENESIN (UNII: I670DAL4SZ)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
- WATER (UNII: 059QF0KO0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
What is the NDC to RxNorm Crosswalk for Sanitizing Wipes?
- RxCUI: 1038558 - benzalkonium chloride 0.13 % Medicated Pad
- RxCUI: 1038558 - benzalkonium chloride 1.3 MG/ML Medicated Pad
- RxCUI: 1038558 - benzalkonium chloride 0.13 % Topical Swab
- RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Pad
- RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM 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".