NDC 50865-207 Foaming Instant Hand Sanitizer With Aloe And Vitamin E
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50865 - Kutol Products Company, Inc.
- 50865-207 - Foaming Instant Hand Sanitizer With Aloe And Vitamin E
Product Packages
NDC Code 50865-207-03
Package Description: 208175 mL in 1 DRUM
NDC Code 50865-207-09
Package Description: 3785 mL in 1 BOTTLE, PLASTIC
NDC Code 50865-207-17
Package Description: 50 mL in 1 BOTTLE, PLASTIC
NDC Code 50865-207-24
Package Description: 1000 mL in 1 BAG
NDC Code 50865-207-31
Package Description: 1000 mL in 1 BAG
NDC Code 50865-207-41
Package Description: 1000 mL in 1 BAG
NDC Code 50865-207-78
Package Description: 950 mL in 1 BOTTLE, PLASTIC
NDC Code 50865-207-91
Package Description: 532 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 50865-207?
What are the uses for Foaming Instant Hand Sanitizer With Aloe And Vitamin E?
Which are Foaming Instant Hand Sanitizer With Aloe And Vitamin E UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Foaming Instant Hand Sanitizer With Aloe And Vitamin E 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)
- EDETATE SODIUM (UNII: MP1J8420LU)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
What is the NDC to RxNorm Crosswalk for Foaming Instant Hand Sanitizer With Aloe And Vitamin E?
- RxCUI: 1049254 - benzalkonium chloride 0.13 % Topical Solution
- RxCUI: 1049254 - benzalkonium chloride 1.3 MG/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".