NDC 55118-605 Truist Sunscreen Moisturizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55118 - Kimberly-clark
- 55118-605 - Truist Sunscreen Moisturizer
Product Packages
NDC Code 55118-605-11
Package Description: 44 mL in 1 BOTTLE, PLASTIC
NDC Code 55118-605-77
Package Description: 118 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 55118-605?
What are the uses for Truist Sunscreen Moisturizer?
Which are Truist Sunscreen Moisturizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Truist Sunscreen Moisturizer 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)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- GLYCERIN (UNII: PDC6A3C0OX)
- TROPAEOLUM MAJUS (UNII: 9G6ZOS4L87)
- ARABICA COFFEE BEAN (UNII: 3SW678MX72)
- ZANTHOXYLUM ARMATUM VAR. ARMATUM FRUIT (UNII: ER3FV125H7)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- ASIATICOSIDE (UNII: PKO39VY215)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- TRIBEHENIN PEG-20 ESTERS (UNII: 84K9EH29Y9)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CHLORPHENESIN (UNII: I670DAL4SZ)
* 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".