NDC 76885-004 Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 76885-004-01
Package Description: 60 mL in 1 BOTTLE
NDC Code 76885-004-02
Package Description: 120 mL in 1 BOTTLE
NDC Code 76885-004-03
Package Description: 236.58 mL in 1 BOTTLE
NDC Code 76885-004-04
Package Description: 354 mL in 1 BOTTLE
NDC Code 76885-004-05
Package Description: 500 mL in 1 BOTTLE
NDC Code 76885-004-06
Package Description: 754.125 mL in 1 BOTTLE
NDC Code 76885-004-07
Package Description: 1000 mL in 1 BOTTLE
NDC Code 76885-004-08
Package Description: 3785 mL in 1 BOTTLE
NDC Code 76885-004-09
Package Description: 208198 mL in 1 DRUM
NDC Code 76885-004-10
Package Description: 1040988.24 mL in 1 CONTAINER
NDC Code 76885-004-11
Package Description: 18927.1 mL in 1 BOX
Product Details
What is NDC 76885-004?
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)
What is the NDC to RxNorm Crosswalk for Hand Sanitizer?
- RxCUI: 1039339 - ethanol 80 % Topical Solution
- RxCUI: 1039339 - ethanol 0.8 ML/ML Topical Solution
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[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".