NDC 79508-020 Doc Hygiene Extra Strength Sanitizing Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 79508 - Blue Flame Medical Llc
- 79508-020 - Doc Hygiene Extra Strength Sanitizing Wipes
Product Packages
NDC Code 79508-020-01
Package Description: 10 PACKAGE in 1 PACKET / 5.94 g in 1 PACKAGE
NDC Code 79508-020-02
Package Description: 35 PACKAGE in 1 CANISTER / 7.92 g in 1 PACKAGE
Product Details
What is NDC 79508-020?
What are the uses for Doc Hygiene Extra Strength Sanitizing Wipes?
Which are Doc Hygiene Extra Strength 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 Doc Hygiene Extra Strength 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:
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLIHEXANIDE HYDROCHLORIDE (UNII: 4XI6112496)
- WATER (UNII: 059QF0KO0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALCOHOL (UNII: 3K9958V90M)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- LEMON TERPENES (UNII: 5DHA4TVW63)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
What is the NDC to RxNorm Crosswalk for Doc Hygiene Extra Strength Sanitizing 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".