NDC 77136-300 80% Alcohol Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77136 - Midland Products Llc
- 77136-300 - 80% Alcohol Hand Sanitizer
Product Packages
NDC Code 77136-300-02
Package Description: 59 mL in 1 BOTTLE, DISPENSING
NDC Code 77136-300-05
Package Description: 18927.1 mL in 1 PAIL
NDC Code 77136-300-08
Package Description: 236.5 mL in 1 BOTTLE, DISPENSING
NDC Code 77136-300-10
Package Description: 3785.4 mL in 1 JUG
NDC Code 77136-300-12
Package Description: 354.8 mL in 1 BOTTLE, PLASTIC
NDC Code 77136-300-16
Package Description: 473.1 mL in 1 BOTTLE, DISPENSING
NDC Code 77136-300-24
Package Description: 709.7 mL in 1 BOTTLE, PLASTIC
NDC Code 77136-300-55
Package Description: 208197.6 mL in 1 DRUM
NDC Code 77136-300-75
Package Description: 1040988.2 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
Product Details
What is NDC 77136-300?
What are the uses for 80% Alcohol Hand Sanitizer?
Which are 80% Alcohol 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 80% Alcohol 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)
* 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".