NDC 30805-007 Symmetry Non-alcohol Foaming Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 30805 - Buckeye International, Inc.
- 30805-007 - Symmetry Non-alcohol Foaming Hand Sanitizer
Product Packages
NDC Code 30805-007-02
Package Description: 1250 mL in 1 BAG
NDC Code 30805-007-07
Package Description: 550 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 30805-007?
What are the uses for Symmetry Non-alcohol Foaming Hand Sanitizer?
Which are Symmetry Non-alcohol Foaming Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Symmetry Non-alcohol Foaming 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:
- WATER (UNII: 059QF0KO0R)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- ALLANTOIN (UNII: 344S277G0Z)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
- EDETATE SODIUM (UNII: MP1J8420LU)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
What is the NDC to RxNorm Crosswalk for Symmetry Non-alcohol Foaming Hand Sanitizer?
- RxCUI: 1049295 - benzalkonium chloride 0.24 % Topical Foam
- RxCUI: 1049295 - benzalkonium chloride 2.4 MG/ML Topical Foam
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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".