NDC 63712-123 Daily Defence Sunscreen Broad Spectrum Spf30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63712 - Zelens Limited
- 63712-123 - Daily Defence Sunscreen Broad Spectrum Spf30
Product Characteristics
Product Packages
NDC Code 63712-123-01
Package Description: 1 TUBE in 1 BOX / 50 mL in 1 TUBE
Product Details
What is NDC 63712-123?
What are the uses for Daily Defence Sunscreen Broad Spectrum Spf30?
Which are Daily Defence Sunscreen Broad Spectrum Spf30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Daily Defence Sunscreen Broad Spectrum Spf30 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)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PERILLA FRUTESCENS TOP (UNII: T4L5881Y68)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- ECHINACEA ANGUSTIFOLIA LEAF (UNII: FS7G8S6PJ8)
- GINKGO (UNII: 19FUJ2C58T)
- PINUS STROBUS BARK (UNII: 8PJ4761097)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- SORBITOL (UNII: 506T60A25R)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- SORBIC ACID (UNII: X045WJ989B)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
* 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".