NDC 68105-003 Jurlique Moisturizing Hand Sanitizer Natural Antibacterial
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Product Details
What is NDC 68105-003?
What are the uses for Jurlique Moisturizing Hand Sanitizer Natural Antibacterial?
Which are Jurlique Moisturizing Hand Sanitizer Natural Antibacterial UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Jurlique Moisturizing Hand Sanitizer Natural Antibacterial 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)
- SAFFLOWER (UNII: 4VBL71TY4Y)
- EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)
- ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- MENTHA PIPERITA LEAF (UNII: A389O33LX6)
- MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)
- SWEET MARJORAM OIL (UNII: ICH7BE016E)
- ROSEMARY (UNII: IJ67X351P9)
- SAGE (UNII: 065C5D077J)
- URTICA DIOICA LEAF (UNII: X6M0DRN46Q)
- GLYCERIN (UNII: PDC6A3C0OX)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
What is the NDC to RxNorm Crosswalk for Jurlique Moisturizing Hand Sanitizer Natural Antibacterial?
- RxCUI: 637077 - ethanol 62 % Topical Lotion
- RxCUI: 637077 - ethanol 0.62 ML/ML Topical Lotion
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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".