NDC 75158-005 Germ Shark Px7 Antibacterial Hand Sanitizer Lemon Scented
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75158 - Germ Shark, Llc
- 75158-005 - Germ Shark Px7 Antibacterial Hand Sanitizer Lemon Scented
Product Packages
NDC Code 75158-005-01
Package Description: 3790 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 75158-005?
What are the uses for Germ Shark Px7 Antibacterial Hand Sanitizer Lemon Scented?
Which are Germ Shark Px7 Antibacterial Hand Sanitizer Lemon Scented UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Germ Shark Px7 Antibacterial Hand Sanitizer Lemon Scented 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 INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- LAURYL LACTATE (UNII: G5SU0BFK7O)
- MYRISTYL LACTATE (UNII: 1D822OC34X)
- CETYL LACTATE (UNII: A7EVH2RK4O)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
What is the NDC to RxNorm Crosswalk for Germ Shark Px7 Antibacterial Hand Sanitizer Lemon Scented?
- RxCUI: 581662 - ethanol 70 % Topical Gel
- RxCUI: 581662 - ethanol 0.7 ML/ML Topical Gel
- RxCUI: 581662 - ethyl alcohol 70 % 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".