NDC 68105-006 Jurlique Spf40 High Protection Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 68105-006?
What are the uses for Jurlique Spf40 High Protection Sunscreen?
Which are Jurlique Spf40 High Protection Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Jurlique Spf40 High Protection 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)
- PHENOXYETHYL CAPRYLATE (UNII: GMI5AN7T8U)
- ETHYL ACRYLATE/METHACRYLIC ACID/STEARETH-20 METHACRYLATE COPOLYMER (UNII: EPA1872R1N)
- GLYCERIN (UNII: PDC6A3C0OX)
- ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- COPOVIDONE K25-31 (UNII: D9C330MD8B)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- MYRISTYL MYRISTATE (UNII: 4042ZC00DY)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- ASCOPHYLLUM NODOSUM (UNII: 168S4EO8YJ)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M)
- PORPHYRA UMBILICALIS (UNII: 14AN0J70WO)
- CORIANDER (UNII: 1OV56052IK)
- CHAMOMILE (UNII: FGL3685T2X)
- ROSA GALLICA FLOWER (UNII: X8W61WUV70)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- VIOLA ODORATA (UNII: AET12U8B74)
- VIOLA TRICOLOR (UNII: 9Q24RAI43V)
- EUROPEAN ELDERBERRY (UNII: BQY1UBX046)
- BANCHA TEA LEAF/TWIG (UNII: EWI42IEH1C)
- CUCUMBER (UNII: YY7C30VXJT)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ALCOHOL (UNII: 3K9958V90M)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- PHYTATE SODIUM (UNII: 88496G1ERL)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
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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".