NDC 49889-1906 Germ Crusher Hand Sanitizer Wipes Germ Crusher
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49889 - Gms Industrial Supply, Inc.
- 49889-1906 - Germ Crusher Hand Sanitizer Wipes
Product Packages
NDC Code 49889-1906-0
Package Description: 4 mL in 1 PACKET
NDC Code 49889-1906-1
Package Description: 438 mL in 1 CONTAINER
NDC Code 49889-1906-2
Package Description: 77 mL in 1 PACKAGE
NDC Code 49889-1906-3
Package Description: 206 mL in 1 CONTAINER
NDC Code 49889-1906-4
Package Description: 619 mL in 1 CONTAINER
NDC Code 49889-1906-5
Package Description: 1134 mL in 1 CONTAINER
NDC Code 49889-1906-6
Package Description: 1247 mL in 1 CONTAINER
Product Details
What is NDC 49889-1906?
What are the uses for Germ Crusher Hand Sanitizer Wipes Germ Crusher?
Which are Germ Crusher Hand Sanitizer Wipes Germ Crusher UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- BENZETHONIUM (UNII: 1VU15B70BP) (Active Moiety)
Which are Germ Crusher Hand Sanitizer Wipes Germ Crusher 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- MINERAL OIL (UNII: T5L8T28FGP)
What is the NDC to RxNorm Crosswalk for Germ Crusher Hand Sanitizer Wipes Germ Crusher?
- RxCUI: 1038764 - benzalkonium Cl 0.1 % / benzethonium Cl 0.1 % Medicated Pad
- RxCUI: 1038764 - benzalkonium chloride 1 MG/ML / benzethonium chloride 1 MG/ML Medicated Pad
- RxCUI: 1038764 - benzalkonium chloride 0.1 % / benzethonium chloride 0.1 % Medicated Pad
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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".