NDC 64521-5678 Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-sterile Solution
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64521 - Sarkli-repechage, Ltd.
- 64521-5678 - Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-sterile Solution
Product Packages
NDC Code 64521-5678-1
Package Description: 473 mL in 1 BOTTLE
NDC Code 64521-5678-2
Package Description: 59 mL in 1 BOTTLE, SPRAY
NDC Code 64521-5678-4
Package Description: 118 mL in 1 BOTTLE, SPRAY
NDC Code 64521-5678-8
Package Description: 236 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 64521-5678?
What are the uses for Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-sterile Solution?
Which are Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-sterile Solution UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-sterile Solution 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)
- WATER (UNII: 059QF0KO0R)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
What is the NDC to RxNorm Crosswalk for Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-sterile Solution?
- 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".