NDC 76744-250 Jejuon Pure Clean Hand Gel
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 76744-250?
Which are Jejuon Pure Clean Hand Gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Jejuon Pure Clean Hand Gel 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- TANGERINE (UNII: KH3E3096OO)
- GLYCERIN (UNII: PDC6A3C0OX)
- HONEY (UNII: Y9H1V576FH)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- LAVANDIN OIL (UNII: 9RES347CKG)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM CARBONATE (UNII: 45P3261C7T)
- NELUMBO NUCIFERA LEAF (UNII: 60C608DPVT)
- TURMERIC (UNII: 856YO1Z64F)
- PANTHENOL (UNII: WV9CM0O67Z)
- ORANGE OIL (UNII: AKN3KSD11B)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)
- ROSEMARY (UNII: IJ67X351P9)
- LIME OIL (UNII: UZH29XGA8G)
- JUNIPERUS DEPPEANA WOOD OIL (UNII: 4739QA5686)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- WATER (UNII: 059QF0KO0R)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
What is the NDC to RxNorm Crosswalk for Jejuon Pure Clean Hand Gel?
- RxCUI: 1049228 - benzalkonium chloride 0.1 % Topical Gel
- RxCUI: 1049228 - benzalkonium chloride 0.001 MG/MG 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".