NDC 74152-001 Cajun Spirits Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 74152 - Cajun Spirits Distillery, Llc
- 74152-001 - Cajun Spirits Hand Sanitizer
Product Packages
NDC Code 74152-001-01
Package Description: 29.6 mL in 1 BOTTLE, PLASTIC
NDC Code 74152-001-02
Package Description: 59.1 mL in 1 BOTTLE, PLASTIC
NDC Code 74152-001-04
Package Description: 118.3 mL in 1 BOTTLE, PLASTIC
NDC Code 74152-001-05
Package Description: 18927 mL in 1 PAIL
NDC Code 74152-001-06
Package Description: 177.4 mL in 1 BOTTLE, PLASTIC
NDC Code 74152-001-08
Package Description: 236.6 mL in 1 BOTTLE, PLASTIC
NDC Code 74152-001-16
Package Description: 473 mL in 1 BOTTLE, PLASTIC
NDC Code 74152-001-18
Package Description: 1893 mL in 1 JUG
NDC Code 74152-001-32
Package Description: 946 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 74152-001?
What are the uses for Cajun Spirits Hand Sanitizer?
Which are Cajun Spirits 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 Cajun Spirits 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:
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- WATER (UNII: 059QF0KO0R)
- GLYCEROL FORMAL (UNII: 3L7GR2604E)
What is the NDC to RxNorm Crosswalk for Cajun Spirits Hand Sanitizer?
- RxCUI: 1039339 - ethanol 80 % Topical Solution
- RxCUI: 1039339 - ethanol 0.8 ML/ML Topical Solution
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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".