NDC 20276-054 Lucky Hand Sanitizer Citrus Zest
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 20276 - Delta Brands Inc.
- 20276-054 - Lucky
Product Packages
NDC Code 20276-054-08
Package Description: 236 mL in 1 BOTTLE, PUMP
NDC Code 20276-054-10
Package Description: 295 mL in 1 BOTTLE, PUMP
NDC Code 20276-054-12
Package Description: 355 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 20276-054?
What are the uses for Lucky Hand Sanitizer Citrus Zest?
Which are Lucky Hand Sanitizer Citrus Zest UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Lucky Hand Sanitizer Citrus Zest 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:
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Lucky Hand Sanitizer Citrus Zest?
- RxCUI: 582753 - ethanol 70 % Topical Solution
- RxCUI: 582753 - ethanol 0.7 ML/ML Topical Solution
- RxCUI: 582753 - ethyl alcohol 70 % Topical Solution
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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".