NDC 72284-0010 Im Derma Relief Sunstick
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72284 - Normalest Co., Ltd.
- 72284-0010 - Im Derma Relief Sunstick
Product Characteristics
Product Packages
NDC Code 72284-0010-1
Package Description: 1 CONTAINER in 1 BOX / 15 g in 1 CONTAINER
Product Details
What is NDC 72284-0010?
Which are Im Derma Relief Sunstick UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Im Derma Relief Sunstick 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:
- HYALURONIC ACID (UNII: S270N0TRQY)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PARAFFIN (UNII: I9O0E3H2ZE)
- TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI)
- VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- CANDELILLA WAX (UNII: WL0328HX19)
- METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- POLYGLYCERYL-10 OLEATE (UNII: 55C81W76DH)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- ADENOSINE (UNII: K72T3FS567)
- MADECASSOSIDE (UNII: CQ2F5O6YIY)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
* Please review the disclaimer below.
[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".