NDC 70897-012 Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 70897-012-01
Package Description: 60 mL in 1 BOTTLE
NDC Code 70897-012-02
Package Description: 50 mL in 1 BOTTLE
NDC Code 70897-012-03
Package Description: 80 mL in 1 BOTTLE
NDC Code 70897-012-04
Package Description: 100 mL in 1 BOTTLE
NDC Code 70897-012-05
Package Description: 120 mL in 1 BOTTLE
NDC Code 70897-012-06
Package Description: 200 mL in 1 BOTTLE
NDC Code 70897-012-07
Package Description: 250 mL in 1 BOTTLE
NDC Code 70897-012-08
Package Description: 300 mL in 1 BOTTLE
NDC Code 70897-012-09
Package Description: 500 mL in 1 BOTTLE
NDC Code 70897-012-10
Package Description: 1000 mL in 1 BOTTLE
NDC Code 70897-012-11
Package Description: 5000 mL in 1 BOTTLE
NDC Code 70897-012-12
Package Description: 3780 mL in 1 BOTTLE
Product Details
What is NDC 70897-012?
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 INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- WATER (UNII: 059QF0KO0R)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- TROLAMINE (UNII: 9O3K93S3TK)
- PEG-40 SORBITAN DIISOSTEARATE (UNII: JL4CCU7I1G)
What is the NDC to RxNorm Crosswalk for Hand Sanitizer?
- RxCUI: 581662 - ethanol 70 % Topical Gel
- RxCUI: 581662 - ethanol 0.7 ML/ML Topical Gel
- RxCUI: 581662 - ethyl alcohol 70 % 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".