NDC 75778-006 Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75778 - Audy Global Enterprises Inc.
- 75778-006 - Hand Sanitizer
Product Packages
NDC Code 75778-006-30
Package Description: 1 PACKAGE in 1 PACKAGE, COMBINATION / 3 BOTTLE in 1 PACKAGE / 45 mL in 1 BOTTLE
NDC Code 75778-006-31
Package Description: 1 PACKAGE in 1 PACKAGE, COMBINATION / 3 BOTTLE in 1 PACKAGE / 45 mL in 1 BOTTLE
Product Details
What is NDC 75778-006?
What are the uses for Hand Sanitizer?
Which are Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Hand Sanitizer 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:
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
- WATER (UNII: 059QF0KO0R)
- CITRUS AURANTIFOLIA SEED OIL (UNII: EW089HAI77)
- LEMON OIL, TERPENELESS (UNII: X69W83NI7V)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GLYCERETH-26 (UNII: NNE56F2N14)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- CITRAL (UNII: T7EU0O9VPP)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
What is the NDC to RxNorm Crosswalk for Hand Sanitizer?
- RxCUI: 1039708 - ethanol 67 % Topical Gel
- RxCUI: 1039708 - ethanol 0.67 ML/ML Topical Gel
* Please review the disclaimer below.
[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".