NDC 59078-122 Tonymoly My Sunny Watery Sun Gel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59078 - Tonymoly Co., Ltd.
- 59078-122 - Tonymoly My Sunny Watery Sun Gel
Product Packages
NDC Code 59078-122-01
Package Description: 1 CONTAINER in 1 CARTON / 45 g in 1 CONTAINER
Product Details
What is NDC 59078-122?
What are the uses for Tonymoly My Sunny Watery Sun Gel?
Which are Tonymoly My Sunny Watery Sun Gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
Which are Tonymoly My Sunny Watery Sun 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:
- TROLAMINE (UNII: 9O3K93S3TK)
- OREGANO (UNII: 0E5AT8T16U)
- CHINESE CINNAMON (UNII: WS4CQ062KM)
- NYMPHAEA ALBA FLOWER (UNII: 40KQ7Q535O)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- WATER (UNII: 059QF0KO0R)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- ALLANTOIN (UNII: 344S277G0Z)
- C12-13 PARETH-23 (UNII: J1WW1510L4)
- C12-13 PARETH-3 (UNII: DMC6N3419L)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CETETH-10 (UNII: LF9X1PN3XJ)
- PEG/PPG-30/10 DIMETHICONE (UNII: J5JO20R8LH)
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- AMILOXATE (UNII: 376KTP06K8)
- CHAMAECYPARIS OBTUSA LEAF (UNII: 7OL154J5XB)
- OCTISALATE (UNII: 4X49Y0596W)
- DOCOSANOL (UNII: 9G1OE216XY)
- WILLOW BARK (UNII: S883J9JDYX)
- PORTULACA OLERACEA WHOLE (UNII: D5J3623SV2)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PLATINUM (UNII: 49DFR088MY)
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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".