NDC 75816-375 Aloe Vera Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75816 - Classic Coatings Systems
- 75816-375 - Aloe Vera Hand Sanitizer
Product Packages
NDC Code 75816-375-01
Package Description: 3785 mL in 1 JUG
NDC Code 75816-375-05
Package Description: 18927 mL in 1 PAIL
NDC Code 75816-375-06
Package Description: 177 mL in 1 BOTTLE, DISPENSING
NDC Code 75816-375-27
Package Description: 1040988 mL in 1 CONTAINER
NDC Code 75816-375-32
Package Description: 946 mL in 1 BOTTLE, DISPENSING
NDC Code 75816-375-55
Package Description: 208198 mL in 1 DRUM
Product Details
What is NDC 75816-375?
What are the uses for Aloe Vera Hand Sanitizer?
Which are Aloe Vera Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
Which are Aloe Vera 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)
What is the NDC to RxNorm Crosswalk for Aloe Vera Hand Sanitizer?
- RxCUI: 1039900 - isopropyl alcohol 75 % Topical Solution
- RxCUI: 1039900 - isopropyl alcohol 0.75 ML/ML Topical Solution
* 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".