NDC 75230-001 Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 75230-001-01
Package Description: 60 BOX in 1 CARTON / 1 BOTTLE in 1 BOX / 37 mL in 1 BOTTLE
NDC Code 75230-001-02
Package Description: 120 BOX in 1 CARTON / 1 BOTTLE in 1 BOX / 37 mL in 1 BOTTLE
NDC Code 75230-001-03
Package Description: 3 CARTON in 1 CARTON / 60 BOX in 1 CARTON / 1 BOTTLE in 1 BOX / 37 mL in 1 BOTTLE
NDC Code 75230-001-04
Package Description: 18 BOTTLE in 1 CARTON / 153 mL in 1 BOTTLE
NDC Code 75230-001-05
Package Description: 24 BOTTLE in 1 CARTON / 153 mL in 1 BOTTLE
NDC Code 75230-001-06
Package Description: 30 BOTTLE in 1 CARTON / 153 mL in 1 BOTTLE
NDC Code 75230-001-07
Package Description: 48 BOTTLE in 1 CARTON / 153 mL in 1 BOTTLE
NDC Code 75230-001-08
Package Description: 18 BOTTLE in 1 CARTON / 307 mL in 1 BOTTLE
NDC Code 75230-001-09
Package Description: 24 BOTTLE in 1 CARTON / 307 mL in 1 BOTTLE
NDC Code 75230-001-10
Package Description: 54 BOTTLE in 1 CARTON / 153 mL in 1 BOTTLE
Product Details
What is NDC 75230-001?
What are the uses for Hand Sanitizer?
Which are 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 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- TOCOPHERYL RETINOATE (UNII: 0WN694NBMM)
- CARBOMER 934 (UNII: Z135WT9208)
- TRIETHANOLAMINE BENZOATE (UNII: M3EN4GC19W)
What is the NDC to RxNorm Crosswalk for Hand Sanitizer?
- RxCUI: 902574 - ethanol 65 % Topical Gel
- RxCUI: 902574 - ethanol 0.65 ML/ML Topical Gel
- RxCUI: 902574 - ethyl alcohol 65 % 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".