NDC 79627-001 Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 79627 - Luster Products, Inc.
- 79627-001 - Hand Sanitizer
Product Characteristics
Product Packages
NDC Code 79627-001-01
Package Description: 59 mL in 1 BOTTLE, PLASTIC
NDC Code 79627-001-02
Package Description: 177 mL in 1 BOTTLE, PLASTIC
NDC Code 79627-001-03
Package Description: 359 mL in 1 BOTTLE, PLASTIC
NDC Code 79627-001-04
Package Description: 473 mL in 1 BOTTLE, PLASTIC
NDC Code 79627-001-05
Package Description: 3784 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 79627-001?
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:
- AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- 1-(2,3,8,8-TETRAMETHYL-1,2,3,4,5,6,7,8-OCTAHYDRONAPHTHALEN-2-YL)ETHANONE (UNII: 1GD7ODM28Y)
- ACETYL CEDRENE (UNII: X6I62755AK)
- ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)
- METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GLYCERIN (UNII: PDC6A3C0OX)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- SANDALORE (UNII: 1XL3NL51UU)
- LEMON OIL (UNII: I9GRO824LL)
- ETHYL MALTOL (UNII: L6Q8K29L05)
What is the NDC to RxNorm Crosswalk for Hand Sanitizer?
- RxCUI: 581662 - ethanol 70 % Topical Gel
- RxCUI: 581662 - ethanol 0.7 ML/ML Topical Gel
- RxCUI: 581662 - ethyl alcohol 70 % 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".