NDC 80065-000 Dewmed Antibacterial Advanced Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 80065 - Dewmed, Llc
- 80065-000 - Dewmed Antibacterial Advanced Hand Sanitizer
Product Packages
NDC Code 80065-000-01
Package Description: 750 mL in 1 BOTTLE
Product Details
What is NDC 80065-000?
What are the uses for Dewmed Antibacterial Advanced Hand Sanitizer?
Which are Dewmed Antibacterial Advanced Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Dewmed Antibacterial Advanced Hand Sanitizer 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)
- POLYQUATERNIUM-37 (10000 MPA.S) (UNII: 41QWS48DFN)
- GLYCERIN (UNII: PDC6A3C0OX)
- PANTHENOL (UNII: WV9CM0O67Z)
- NIACINAMIDE (UNII: 25X51I8RD4)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TEA TREE OIL (UNII: VIF565UC2G)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Dewmed Antibacterial Advanced Hand Sanitizer?
- RxCUI: 1049228 - benzalkonium chloride 0.1 % Topical Gel
- RxCUI: 1049228 - benzalkonium chloride 0.001 MG/MG Topical Gel
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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".