NDC 78919-102 Kac Zapx Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 78919 - Klein Anderson Corp
- 78919-102 - Kac Zapx Hand Sanitizer
Product Packages
NDC Code 78919-102-02
Package Description: 59.14 mL in 1 BOTTLE, PLASTIC
NDC Code 78919-102-03
Package Description: 88.72 mL in 1 BOTTLE, PLASTIC
NDC Code 78919-102-08
Package Description: 236.59 mL in 1 BOTTLE, PLASTIC
NDC Code 78919-102-32
Package Description: 946.35 mL in 1 BOTTLE, PLASTIC
NDC Code 78919-102-64
Package Description: 1892.71 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 78919-102?
What are the uses for Kac Zapx Hand Sanitizer?
Which are Kac Zapx 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 Kac Zapx 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:
- MONOETHANOLAMINE (UNII: 5KV86114PT)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Kac Zapx Hand Sanitizer?
- RxCUI: 2277550 - ethanol 72 % Topical Gel
- RxCUI: 2277550 - ethanol 0.72 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".