NDC 43196-207 Foaming Instant Hand Sanitizer With Aloe And Vitamin E
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What is NDC 43196-207?
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:
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- BENZETHONIUM (UNII: 1VU15B70BP) (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)
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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".