NDC 73892-0004 Flint Clean Hands Hand Sanitizer Gel (ethanol)
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73892 - Juhwanbio.cell Co.,ltd.
- 73892-0004 - Flint Clean Hands Hand Sanitizer Gel (ethanol)
Product Packages
NDC Code 73892-0004-2
Package Description: 500 mL in 1 BOTTLE
NDC Code 73892-0004-3
Package Description: 1000 mL in 1 BOTTLE
NDC Code 73892-0004-4
Package Description: 3785 mL in 1 BOTTLE
Product Details
What is NDC 73892-0004?
What are the uses for Flint Clean Hands Hand Sanitizer Gel (ethanol)?
Which are Flint Clean Hands Hand Sanitizer Gel (ethanol) UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Flint Clean Hands Hand Sanitizer Gel (ethanol) 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)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- TROLAMINE (UNII: 9O3K93S3TK)
- HYALURONIC ACID (UNII: S270N0TRQY)
What is the NDC to RxNorm Crosswalk for Flint Clean Hands Hand Sanitizer Gel (ethanol)?
- RxCUI: 2369931 - ethanol 74.2 % Topical Gel
- RxCUI: 2369931 - ethanol 0.742 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".