NDC 42421-692 Desert Fusion Nutritious Olive Leaf Daily Defense Broad Spectrum Spf 15 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42421 - Emilia Personal Care Inc.
- 42421-692 - Desert Fusion Nutritious Olive Leaf Daily Defense Broad Spectrum Spf 15 Sunscreen
Product Packages
NDC Code 42421-692-12
Package Description: 1 JAR in 1 CARTON / 50 g in 1 JAR
Product Details
What is NDC 42421-692?
What are the uses for Desert Fusion Nutritious Olive Leaf Daily Defense Broad Spectrum Spf 15 Sunscreen?
Which are Desert Fusion Nutritious Olive Leaf Daily Defense Broad Spectrum Spf 15 Sunscreen 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)
Which are Desert Fusion Nutritious Olive Leaf Daily Defense Broad Spectrum Spf 15 Sunscreen 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 5 (UNII: 0THT5PCI0R)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- STEARETH-2 (UNII: V56DFE46J5)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- DOCOSANOL (UNII: 9G1OE216XY)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- STEARETH-21 (UNII: 53J3F32P58)
- GLYCERIN (UNII: PDC6A3C0OX)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TRIETHYLENE GLYCOL (UNII: 3P5SU53360)
- POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SOY ISOFLAVONES (UNII: 71B37NR06D)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- PORPHYRA UMBILICALIS (UNII: 14AN0J70WO)
- PANTHENOL (UNII: WV9CM0O67Z)
- OPUNTIA STREPTACANTHA STEM (UNII: 3TF9Z1U73O)
- SHEA BUTTER (UNII: K49155WL9Y)
- OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- JOJOBA OIL (UNII: 724GKU717M)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- TROLAMINE (UNII: 9O3K93S3TK)
* 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".