NDC 62742-4073 Derma Brilliance Sunscreen Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62742 - Allure Labs, Inc
- 62742-4073 - Derma Brilliance Sunscreen Spf 30
Product Packages
NDC Code 62742-4073-1
Package Description: 28.3 g in 1 TUBE
Product Details
What is NDC 62742-4073?
What are the uses for Derma Brilliance Sunscreen Spf 30?
Which are Derma Brilliance Sunscreen Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (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 Derma Brilliance Sunscreen Spf 30 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- KIWI FRUIT (UNII: 71ES77LGJC)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- TEPRENONE (UNII: S8S8451A4O)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- LAURYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EX0F4CZ66H)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PALMITOYL PENTAPEPTIDE-4 (UNII: KK181SM5JG)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYGONUM AVICULARE TOP (UNII: ZCD6009IUF)
- ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- ARABIDOPSIS THALIANA (UNII: AI3L60HQ81)
- UBIDECARENONE (UNII: EJ27X76M46)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- TROLAMINE (UNII: 9O3K93S3TK)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
* 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".