NDC 51209-013 Covex Antibacterial Hand Sanitizer, Fresh Aloe
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51209 - Dalan Kimya Endustri Anonim Sirketi
- 51209-013 - Covex Antibacterial Hand Sanitizer, Fresh Aloe
Product Packages
NDC Code 51209-013-00
Package Description: 236 mL in 1 BOTTLE
Product Details
What is NDC 51209-013?
What are the uses for Covex Antibacterial Hand Sanitizer, Fresh Aloe?
Which are Covex Antibacterial Hand Sanitizer, Fresh Aloe UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Covex Antibacterial Hand Sanitizer, Fresh Aloe 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- TROLAMINE (UNII: 9O3K93S3TK)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SKIM MILK (UNII: 6A001Y4M5A)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- GINGER (UNII: C5529G5JPQ)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- GERANIOL (UNII: L837108USY)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- CITRAL (UNII: T7EU0O9VPP)
What is the NDC to RxNorm Crosswalk for Covex Antibacterial Hand Sanitizer, Fresh Aloe?
- RxCUI: 581658 - ethanol 60 % Topical Gel
- RxCUI: 581658 - ethanol 0.6 ML/ML 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".