NDC 50049-006 Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 50049-006-01
Package Description: 100 BOTTLE in 1 CARTON / 60 mL in 1 BOTTLE
NDC Code 50049-006-02
Package Description: 60 BOTTLE in 1 CARTON / 100 mL in 1 BOTTLE
NDC Code 50049-006-03
Package Description: 24 BOTTLE in 1 CARTON / 250 mL in 1 BOTTLE
NDC Code 50049-006-04
Package Description: 12 BOTTLE in 1 CARTON / 500 mL in 1 BOTTLE
NDC Code 50049-006-05
Package Description: 6 BOTTLE in 1 CARTON / 998 mL in 1 BOTTLE
NDC Code 50049-006-06
Package Description: 36 BOTTLE in 1 CARTON / 180 mL in 1 BOTTLE
NDC Code 50049-006-07
Package Description: 24 BOTTLE in 1 CARTON / 200 mL in 1 BOTTLE
NDC Code 50049-006-08
Package Description: 24 BOTTLE in 1 CARTON / 300 mL in 1 BOTTLE
NDC Code 50049-006-09
Package Description: 100 BOTTLE in 1 CARTON / 50 mL in 1 BOTTLE
NDC Code 50049-006-10
Package Description: 100 BOTTLE in 1 CARTON / 30 mL in 1 BOTTLE
Product Details
What is NDC 50049-006?
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:
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
What is the NDC to RxNorm Crosswalk for Hand Sanitizer?
- RxCUI: 1305100 - ethanol 75 % Topical Gel
- RxCUI: 1305100 - ethanol 0.75 ML/ML 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".