NDC 57691-825 Mango Antibacterial Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 57691-825?
What are the uses for Mango Antibacterial Hand Sanitizer?
Which are Mango Antibacterial Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Mango Antibacterial 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- BETAINE (UNII: 3SCV180C9W)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- MANGO JUICE (UNII: IU6I1JNV24)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- CARBOMER INTERPOLYMER TYPE A (55000 MPA.S) (UNII: 59TL3WG5CO)
- LIMONENE, (+/-)- (UNII: 9MC3I34447)
What is the NDC to RxNorm Crosswalk for Mango Antibacterial Hand Sanitizer?
- RxCUI: 1302342 - ethanol 73.4 % Topical Gel
- RxCUI: 1302342 - ethanol 0.734 ML/ML Topical Gel
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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".