NDC 78662-700 Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 78662 - Rx San Llc
- 78662-700 - Hand Sanitizer
Product Packages
NDC Code 78662-700-01
Package Description: 3785 mL in 1 BOTTLE
NDC Code 78662-700-04
Package Description: 118 mL in 1 BOTTLE, DISPENSING
NDC Code 78662-700-12
Package Description: 355 mL in 1 BOTTLE, DISPENSING
NDC Code 78662-700-16
Package Description: 473 mL in 1 BOTTLE, DISPENSING
NDC Code 78662-700-50
Package Description: 18927 mL in 1 CONTAINER
NDC Code 78662-700-75
Package Description: 1041000 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
Product Details
What is NDC 78662-700?
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:
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- WATER (UNII: 059QF0KO0R)
- TROLAMINE (UNII: 9O3K93S3TK)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
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".