NDC 50563-283 Livegreen Antibacterial Hand Sanitizer Duo Peppermint Scented Aloe Scented
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50563 - Enchante Accessories Inc.
- 50563-283 - Livegreen Antibacterial Hand Sanitizer Duo Peppermint Scented Aloe Scented
Product Packages
NDC Code 50563-283-01
Package Description: 1 KIT in 1 KIT * 30 mL in 1 BOTTLE (50563-281-01) * 30 mL in 1 BOTTLE (50563-282-01)
Product Details
What is NDC 50563-283?
What are the uses for Livegreen Antibacterial Hand Sanitizer Duo Peppermint Scented Aloe Scented?
Which are Livegreen Antibacterial Hand Sanitizer Duo Peppermint Scented Aloe Scented UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Livegreen Antibacterial Hand Sanitizer Duo Peppermint Scented Aloe Scented 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- TROLAMINE (UNII: 9O3K93S3TK)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
What is the NDC to RxNorm Crosswalk for Livegreen Antibacterial Hand Sanitizer Duo Peppermint Scented Aloe Scented?
- RxCUI: 1047755 - ethanol 75 % Topical Solution
- RxCUI: 1047755 - ethanol 0.75 ML/ML 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".