NDC 73107-106 Konix Hand Sanitizer Gel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 73107-106-10
Package Description: 30 mL in 1 BOTTLE
NDC Code 73107-106-11
Package Description: 50 mL in 1 BOTTLE
NDC Code 73107-106-12
Package Description: 85 mL in 1 BOTTLE
NDC Code 73107-106-13
Package Description: 100 mL in 1 BOTTLE
NDC Code 73107-106-14
Package Description: 150 mL in 1 BOTTLE
NDC Code 73107-106-15
Package Description: 200 mL in 1 BOTTLE
NDC Code 73107-106-16
Package Description: 250 mL in 1 BOTTLE
NDC Code 73107-106-17
Package Description: 500 mL in 1 BOTTLE
NDC Code 73107-106-18
Package Description: 1000 mL in 1 BOTTLE
NDC Code 73107-106-19
Package Description: 5000 mL in 1 BOTTLE
NDC Code 73107-106-20
Package Description: 20 mL in 1 PACKET
NDC Code 73107-106-40
Package Description: 5 mL in 1 PACKET
NDC Code 73107-106-41
Package Description: 59 mL in 1 BOTTLE
NDC Code 73107-106-42
Package Description: 118 mL in 1 BOTTLE
NDC Code 73107-106-43
Package Description: 236 mL in 1 BOTTLE
NDC Code 73107-106-44
Package Description: 354 mL in 1 BOTTLE
NDC Code 73107-106-45
Package Description: 473 mL in 1 BOTTLE
NDC Code 73107-106-46
Package Description: 591 mL in 1 BOTTLE
NDC Code 73107-106-47
Package Description: 710 mL in 1 BOTTLE
NDC Code 73107-106-48
Package Description: 946 mL in 1 BOTTLE
NDC Code 73107-106-49
Package Description: 3780 mL in 1 BOTTLE
Product Details
What is NDC 73107-106?
What are the uses for Konix Hand Sanitizer Gel?
Which are Konix Hand Sanitizer Gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Konix Hand Sanitizer Gel 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)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
What is the NDC to RxNorm Crosswalk for Konix Hand Sanitizer Gel?
- 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".