NDC 76680-007 Disposable Disinfectant
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 76680-007-01
Package Description: 30 mL in 1 BOTTLE
NDC Code 76680-007-02
Package Description: 50 mL in 1 BOTTLE
NDC Code 76680-007-03
Package Description: 60 mL in 1 BOTTLE
NDC Code 76680-007-04
Package Description: 80 mL in 1 BOTTLE
NDC Code 76680-007-05
Package Description: 100 mL in 1 BOTTLE
NDC Code 76680-007-06
Package Description: 200 mL in 1 BOTTLE
NDC Code 76680-007-07
Package Description: 300 mL in 1 BOTTLE
NDC Code 76680-007-08
Package Description: 350 mL in 1 BOTTLE
NDC Code 76680-007-09
Package Description: 400 mL in 1 BOTTLE
NDC Code 76680-007-10
Package Description: 480 mL in 1 BOTTLE
NDC Code 76680-007-11
Package Description: 500 mL in 1 BOTTLE
NDC Code 76680-007-12
Package Description: 700 mL in 1 BOTTLE
NDC Code 76680-007-13
Package Description: 5000 mL in 1 BOTTLE
Product Details
What is NDC 76680-007?
What are the uses for Disposable Disinfectant?
Which are Disposable Disinfectant UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Disposable Disinfectant 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:
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- GLYCERIN (UNII: PDC6A3C0OX)
- CARBOMER COPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 1N11AG4X4L)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Disposable Disinfectant?
- RxCUI: 1305100 - ethanol 75 % Topical Gel
- RxCUI: 1305100 - ethanol 0.75 ML/ML Topical Gel
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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".