NDC 59078-120 Tonymoly My Sunny All Sunspray
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 59078-120?
What are the uses for Tonymoly My Sunny All Sunspray?
Which are Tonymoly My Sunny All Sunspray UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Tonymoly My Sunny All Sunspray 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:
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PORTULACA OLERACEA WHOLE (UNII: D5J3623SV2)
- CHINESE CINNAMON (UNII: WS4CQ062KM)
- NYMPHAEA ALBA FLOWER (UNII: 40KQ7Q535O)
- OREGANO (UNII: 0E5AT8T16U)
- WILLOW BARK (UNII: S883J9JDYX)
- PLATINUM (UNII: 49DFR088MY)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- WATER (UNII: 059QF0KO0R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ALCOHOL (UNII: 3K9958V90M)
- PRUNUS MUME FRUIT (UNII: 639190I8CU)
- CHAMAECYPARIS OBTUSA LEAF (UNII: 7OL154J5XB)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
* 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".