NDC 81005-001 Blue Bear Antibacterial Hand Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 81005 - Blue Bear Protection Llc
- 81005-001 - Blue Bear Antibacterial Hand Wipes
Product Packages
NDC Code 81005-001-02
Package Description: 15 PATCH in 1 PACKAGE / .0065835 g in 1 PATCH (81005-001-01)
NDC Code 81005-001-04
Package Description: 100 PATCH in 1 PACKAGE / .010206 g in 1 PATCH (81005-001-03)
NDC Code 81005-001-06
Package Description: 500 PATCH in 1 CANISTER / .0067 g in 1 PATCH (81005-001-05)
NDC Code 81005-001-08
Package Description: 100 PATCH in 1 CANISTER / .0067 g in 1 PATCH (81005-001-07)
Product Details
What is NDC 81005-001?
What are the uses for Blue Bear Antibacterial Hand Wipes?
Which are Blue Bear Antibacterial Hand 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 Blue Bear Antibacterial Hand 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- WATER (UNII: 059QF0KO0R)
- CITRAL (UNII: T7EU0O9VPP)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- GLYCERYL OLEATE (UNII: 4PC054V79P)
- LINALOOL, (+)- (UNII: F4VNO44C09)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ETIDRONATE TETRASODIUM (UNII: CZZ9T1T1X4)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- FATTY-ACID AMIDE HYDROLASE 1 (UNII: E747F394ZQ)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
What is the NDC to RxNorm Crosswalk for Blue Bear Antibacterial Hand Wipes?
- RxCUI: 2375303 - benzalkonium chloride 0.23 % Medicated Pad
- RxCUI: 2375303 - benzalkonium chloride 2.3 MG/ML Medicated Pad
* 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".