NDC 20276-430 Lucky Sanitizing Hand Towels
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 20276 - Delta Brands, Inc
- 20276-430 - Lucky
Product Packages
NDC Code 20276-430-10
Package Description: 10 CLOTH in 1 BOX
Product Details
What is NDC 20276-430?
What are the uses for Lucky Sanitizing Hand Towels?
Which are Lucky Sanitizing Hand Towels UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Lucky Sanitizing Hand Towels 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)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
- TRIDECETH-6 (UNII: 3T5PCR2H0C)
- GLYCERIN (UNII: PDC6A3C0OX)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CORN OIL (UNII: 8470G57WFM)
What is the NDC to RxNorm Crosswalk for Lucky Sanitizing Hand Towels?
- RxCUI: 1041780 - ethanol 62 % Medicated Pad
- RxCUI: 1041780 - ethanol 0.62 ML/ML Medicated Pad
- RxCUI: 1041780 - ethanol 62 % Hand Sanitizer Wipes
- RxCUI: 1041780 - ethanol 62 % Topical Cloth
- RxCUI: 1041780 - ethanol 62 % 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".