NDC 74588-571 Hygienex Hand Sanitizer Liquid Sanitizer With Eucalyptus Oil
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 74588 - Global Impact Innovation Llc
- 74588-571 - Hygienex Hand Sanitizer
Product Packages
NDC Code 74588-571-01
Package Description: 208.198 L in 1 DRUM
NDC Code 74588-571-02
Package Description: 1040 L in 1 DRUM
NDC Code 74588-571-04
Package Description: 3.785 L in 1 BOTTLE
NDC Code 74588-571-05
Package Description: 18.927 L in 1 DRUM
Product Details
What is NDC 74588-571?
What are the uses for Hygienex Hand Sanitizer Liquid Sanitizer With Eucalyptus Oil?
Which are Hygienex Hand Sanitizer Liquid Sanitizer With Eucalyptus Oil UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Hygienex Hand Sanitizer Liquid Sanitizer With Eucalyptus Oil 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:
- EUCALYPTOL (UNII: RV6J6604TK)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Hygienex Hand Sanitizer Liquid Sanitizer With Eucalyptus Oil?
- RxCUI: 1039339 - ethanol 80 % Topical Solution
- RxCUI: 1039339 - ethanol 0.8 ML/ML Topical Solution
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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".