NDC 69078-101 Lacura Face Care Q10 Day Spf-15
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 69078-101?
What are the uses for Lacura Face Care Q10 Day Spf-15?
Which are Lacura Face Care Q10 Day Spf-15 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 Lacura Face Care Q10 Day Spf-15 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)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
- SORBITOL (UNII: 506T60A25R)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PANTHENOL (UNII: WV9CM0O67Z)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- JOJOBA OIL (UNII: 724GKU717M)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- UBIDECARENONE (UNII: EJ27X76M46)
- SODIUM ALGINATE (UNII: C269C4G2ZQ)
- SAMBUCUS NIGRA FLOWER (UNII: 07V4DX094T)
- CARICA PAPAYA WHOLE (UNII: S0U63B0Q51)
- ADENOSINE TRIPHOSPHATE DISODIUM (UNII: 5L51B4DR1G)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- PROPANEDIOL (UNII: 5965N8W85T)
- EDETATE SODIUM TETRAHYDRATE (UNII: L13NHD21X6)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- ALCOHOL (UNII: 3K9958V90M)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- DIMETHYLMETHOXY CHROMANOL (UNII: XBH432G01F)
- GLYCERYL OLEATE (UNII: 4PC054V79P)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
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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".