NDC 72257-250 Fresh Hand Antiseptic Cleaner
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72257 - Province Apothecary Inc
- 72257-250 - Fresh Hand Antiseptic Cleaner
Product Packages
NDC Code 72257-250-01
Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 250 mL in 1 BOTTLE, PLASTIC (72257-250-00)
Product Details
What is NDC 72257-250?
What are the uses for Fresh Hand Antiseptic Cleaner?
Which are Fresh Hand Antiseptic Cleaner UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Fresh Hand Antiseptic Cleaner 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:
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- LAURETH-7 (UNII: Z95S6G8201)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER (UNII: 788QAG3W8A)
What is the NDC to RxNorm Crosswalk for Fresh Hand Antiseptic Cleaner?
- RxCUI: 581658 - ethanol 60 % Topical Gel
- RxCUI: 581658 - ethanol 0.6 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".