NDC 78174-014 Hygieni-klean Hand Sanitizer Gel Fresh
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 78174 - Custom Chemical Services, Llc
- 78174-014 - Hygieni-klean Hand Sanitizer Gel Fresh
Product Packages
NDC Code 78174-014-01
Package Description: 3.78541 L in 1 JUG
NDC Code 78174-014-02
Package Description: .946353 L in 1 BOTTLE
NDC Code 78174-014-03
Package Description: .473176 L in 1 BOTTLE
NDC Code 78174-014-04
Package Description: .354882 L in 1 BOTTLE
NDC Code 78174-014-05
Package Description: .236588 L in 1 BOTTLE
NDC Code 78174-014-06
Package Description: .118294 L in 1 BOTTLE
NDC Code 78174-014-07
Package Description: .0591471 L in 1 BOTTLE
Product Details
What is NDC 78174-014?
What are the uses for Hygieni-klean Hand Sanitizer Gel Fresh?
Which are Hygieni-klean Hand Sanitizer Gel Fresh UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Hygieni-klean Hand Sanitizer Gel Fresh 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9)
- AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (55000 MPA.S) (UNII: F01RIY4371)
- WATER (UNII: 059QF0KO0R)
- FRAGRANCE CUCUMBER ALOE ORC1802955 (UNII: FSS3TH6V9M)
What is the NDC to RxNorm Crosswalk for Hygieni-klean Hand Sanitizer Gel Fresh?
- RxCUI: 1305100 - ethanol 75 % Topical Gel
- RxCUI: 1305100 - ethanol 0.75 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".