NDC 78580-020 Santizall 75 Percent Ethanol Wet Wipe
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 78580 - Glory Co., Ltd.
- 78580-020 - Santizall 75 Percent Ethanol Wet Wipe
Product Packages
NDC Code 78580-020-01
Package Description: 100 CLOTH in 1 PACKET
Product Details
What is NDC 78580-020?
What are the uses for Santizall 75 Percent Ethanol Wet Wipe?
Which are Santizall 75 Percent Ethanol Wet Wipe UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Santizall 75 Percent Ethanol Wet Wipe 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:
- WATER (UNII: 059QF0KO0R)
- CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
- GLYCERIN (UNII: PDC6A3C0OX)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
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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".