NDC 79774-002 Ms. Germsafe Antibacterial Hand Sanitizer -tropical Coconut
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What is NDC 79774-002?
What are the uses for Ms. Germsafe Antibacterial Hand Sanitizer -tropical Coconut?
Which are Ms. Germsafe Antibacterial Hand Sanitizer -tropical Coconut UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Ms. Germsafe Antibacterial Hand Sanitizer -tropical Coconut 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)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BRONOPOL (UNII: 6PU1E16C9W)
- DICHLOROBENZYL ALCOHOL (UNII: 1NKX3648J9)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- GERANIOL (UNII: L837108USY)
- CITRAL (UNII: T7EU0O9VPP)
- .ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)
- BENZYL BENZOATE (UNII: N863NB338G)
- DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
What is the NDC to RxNorm Crosswalk for Ms. Germsafe Antibacterial Hand Sanitizer -tropical Coconut?
- RxCUI: 1041849 - ethanol 70 % Topical Spray
- RxCUI: 1041849 - ethanol 0.7 ML/ML Topical Spray
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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".